A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3476963



Internal ID18720620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16641704hg38UCSC Ensembl
Innerchr1:16871266..16968199hg19UCSC Ensembl
Innerchr1:16743853..16840786hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3896934
hg1996934
hg1896934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013756
Supporting Variants
Samples
Known GenesCROCCP2, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3476963
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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