A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687417



Internal ID15424069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100446711..100448367hg38UCSC Ensembl
Innerchr6:100894587..100896243hg19UCSC Ensembl
Innerchr6:101001308..101002964hg18UCSC Ensembl
Innerchr6:101001308..101002964hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381657
hg191657
hg181657
hg171657
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515895
Supporting Variants
Samples
Known GenesSIM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687417
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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