A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593162



Internal ID18891443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21930369..21970749hg38UCSC Ensembl
Innerchr3:21971861..22012241hg19UCSC Ensembl
Innerchr3:21946865..21987245hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3840381
hg1940381
hg1840381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999478
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)nssv3593162
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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