A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015021



Internal ID19104238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:31747669..31805627hg38UCSC Ensembl
Innerchr2:31972738..32030696hg19UCSC Ensembl
Innerchr2:31826242..31884200hg18UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3857959
hg1957959
hg1857959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579152
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)nsv1015021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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