A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3473239



Internal ID18718691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16561560..16637038hg38UCSC Ensembl
Innerchr1:16888055..16963533hg19UCSC Ensembl
Innerchr1:16760642..16836120hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3875479
hg1975479
hg1875479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012484
Supporting Variants
Samples
Known GenesCROCCP2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3473239
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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