A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154821



Internal ID22085326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30084564..30091000hg38UCSC Ensembl
Outerchr12:30082648..30091017hg38UCSC Ensembl
Innerchr12:30237497..30243933hg19UCSC Ensembl
Outerchr12:30235581..30243950hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388370
hg198370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009018, nssv4009021, nssv4009034, nssv4009015, nssv4008996, nssv4009023, nssv4009010, nssv4008998, nssv4009037, nssv4009001, nssv4009005, nssv4009008, nssv4009017, nssv4009004, nssv4009032, nssv4009030, nssv4009007, nssv4009027, nssv4009031, nssv4009000, nssv4009016, nssv4009013, nssv4009006, nssv4009003, nssv4009028, nssv4009012, nssv4009038, nssv4009029, nssv4009026, nssv4008999, nssv4009024, nssv4009033, nssv4009020, nssv4009036, nssv4008997, nssv4009014, nssv4009025, nssv4009009, nssv4009002, nssv4009022, nssv4009019, nssv4009035, nssv4009011
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154821
Frequency
Sample Size131
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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