A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655753



Internal ID15045719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35337799..35363447hg38UCSC Ensembl
Innerchr17:33664818..33690466hg19UCSC Ensembl
Innerchr17:30688931..30714579hg18UCSC Ensembl
Innerchr17:30688931..30714579hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3825649
hg1925649
hg1825649
hg1725649
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515566
Supporting Variants
Samples
Known GenesSLFN11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655753
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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