A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568613



Internal ID18866894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52876233..52940242hg38UCSC Ensembl
Innerchr17:50953593..51017602hg19UCSC Ensembl
Innerchr17:48308592..48372601hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3864010
hg1964010
hg1864010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056625
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568613
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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