A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3578996



Internal ID18877277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20150990..20177846hg38UCSC Ensembl
Innerchr2:20350751..20377607hg19UCSC Ensembl
Innerchr2:20214232..20241088hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3826857
hg1926857
hg1826857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999131
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)nssv3578996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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