A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3477604



Internal ID18720953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16627264..16643949hg38UCSC Ensembl
Innerchr1:16953759..16970444hg19UCSC Ensembl
Innerchr1:16826346..16843031hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816686
hg1916686
hg1816686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006849
Supporting Variants
Samples
Known GenesCROCCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3477604
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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