A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3464679



Internal ID19060847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17450325..17514495hg38UCSC Ensembl
Innerchr1:17776821..17840991hg19UCSC Ensembl
Innerchr1:17649408..17713578hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3864171
hg1964171
hg1864171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000724
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)nssv3464679
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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