A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705642



Internal ID15095608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17695627..17699091hg38UCSC Ensembl
Innerchr6:17695858..17699322hg19UCSC Ensembl
Innerchr6:17803837..17807301hg18UCSC Ensembl
Innerchr6:17803837..17807301hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383465
hg193465
hg183465
hg173465
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516012
Supporting Variants
Samples
Known GenesNUP153
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705642
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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