A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155378



Internal ID22085883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15140609..15151185hg38UCSC Ensembl
Outerchr17:15134796..15155674hg38UCSC Ensembl
Innerchr17:15043926..15054502hg19UCSC Ensembl
Outerchr17:15038113..15058991hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820879
hg1920879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010097, nssv4010088, nssv4010094, nssv4010095, nssv4010102, nssv4010090, nssv4010092, nssv4010091, nssv4010086, nssv4010100, nssv4010099, nssv4010101, nssv4010087, nssv4010089, nssv4010093, nssv4010098
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155378
Frequency
Sample Size131
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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