A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577106



Internal ID18875387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14642951..14675593hg38UCSC Ensembl
Innerchr2:14783075..14815717hg19UCSC Ensembl
Innerchr2:14700526..14733168hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3832643
hg1932643
hg1832643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010526
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)nssv3577106
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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