A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528128



Internal ID15108735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114276493..115149965hg38UCSC Ensembl
Innerchr6:114597657..115471129hg19UCSC Ensembl
Innerchr6:114704350..115577822hg18UCSC Ensembl
Innerchr6:114704350..115577822hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38873473
hg19873473
hg18873473
hg17873473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704673
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528128
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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