A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579004



Internal ID18877285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21298765..21323987hg38UCSC Ensembl
Innerchr2:21521637..21546859hg19UCSC Ensembl
Innerchr2:21375142..21400364hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3825223
hg1925223
hg1825223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003630
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)nssv3579004
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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