A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006462



Internal ID19095679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14173035..14248959hg38UCSC Ensembl
Innerchr2:14313160..14389083hg19UCSC Ensembl
Innerchr2:14230611..14306534hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3875925
hg1975924
hg1875924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577056, nssv3577055
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)nsv1006462
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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