A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577059



Internal ID18875340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14200165..14232559hg38UCSC Ensembl
Innerchr2:14340289..14372683hg19UCSC Ensembl
Innerchr2:14257740..14290134hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3832395
hg1932395
hg1832395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997320
Supporting Variants
Samples
Known GenesLINC00276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577059
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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