A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682841



Internal ID15072807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357016..35436659hg38UCSC Ensembl
Innerchr17:33684035..33763678hg19UCSC Ensembl
Innerchr17:30708148..30787791hg18UCSC Ensembl
Innerchr17:30708148..30787791hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3879644
hg1979644
hg1879644
hg1779644
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515566
Supporting Variants
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682841
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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