A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495190



Internal ID19082831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208265627..208283580hg38UCSC Ensembl
Innerchr1:208438972..208456925hg19UCSC Ensembl
Innerchr1:206505595..206523548hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3817954
hg1917954
hg1817954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006892
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)nssv3495190
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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