A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729014



Internal ID19027295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88836527..89174336hg38UCSC Ensembl
Innerchr2:89136040..89473820hg19UCSC Ensembl
Innerchr2:88917155..89254935hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38337810
hg19337781
hg18337781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009277
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)nssv3729014
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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