A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155368



Internal ID22085873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88080057..88081785hg38UCSC Ensembl
Outerchr16:88076816..88082524hg38UCSC Ensembl
Innerchr16:88113663..88115391hg19UCSC Ensembl
Outerchr16:88110422..88116130hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385709
hg195709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010038, nssv4010004, nssv4010049, nssv4010012, nssv4010015, nssv4010066, nssv4010010, nssv4010043, nssv4009996, nssv4010069, nssv4010006, nssv4010071, nssv4010037, nssv4010076, nssv4010070, nssv4010035, nssv4010059, nssv4010057, nssv4010042, nssv4010054, nssv4010048, nssv4010046, nssv4010029, nssv4010007, nssv4010034, nssv4010009, nssv4010001, nssv4009995, nssv4010058, nssv4010040, nssv4010064, nssv4010072, nssv4010027, nssv4010005, nssv4010065, nssv4010062, nssv4010036, nssv4010023, nssv4010045, nssv4010051, nssv4010022, nssv4010028, nssv4010020, nssv4010053, nssv4010031, nssv4010013, nssv4009992, nssv4010002, nssv4010068, nssv4010075, nssv4010060, nssv4010061, nssv4010067, nssv4010011, nssv4009998, nssv4010039, nssv4010018, nssv4010047, nssv4010024, nssv4010033, nssv4010050, nssv4010014, nssv4009994, nssv4009993, nssv4010025, nssv4010044, nssv4010017, nssv4010021, nssv4010000, nssv4010056, nssv4010055, nssv4010003, nssv4009999, nssv4010073, nssv4010016, nssv4010026, nssv4010032
Samples
Known GenesBANP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155368
Frequency
Sample Size131
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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