A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528107



Internal ID15455400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76863518..76867144hg38UCSC Ensembl
Innerchr6:77573235..77576861hg19UCSC Ensembl
Innerchr6:77629954..77633580hg18UCSC Ensembl
Innerchr6:77629954..77633580hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383627
hg193627
hg183627
hg173627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704648
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528107
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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