A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687242



Internal ID15077208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357016..35441180hg38UCSC Ensembl
Innerchr17:33684035..33768199hg19UCSC Ensembl
Innerchr17:30708148..30792312hg18UCSC Ensembl
Innerchr17:30708148..30792312hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3884165
hg1984165
hg1884165
hg1784165
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)nssv687242
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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