A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704714



Internal ID15441366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57239468..57265776hg38UCSC Ensembl
Innerchr6:57104266..57130574hg19UCSC Ensembl
Innerchr6:57212225..57238533hg18UCSC Ensembl
Innerchr6:57212225..57238533hg17UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3826309
hg1926309
hg1826309
hg1726309
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528165
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704714
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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