A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579013



Internal ID18877294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22524861..22565896hg38UCSC Ensembl
Innerchr2:22747733..22788768hg19UCSC Ensembl
Innerchr2:22601238..22642273hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3841036
hg1941036
hg1841036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999402
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)nssv3579013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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