A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999868



Internal ID19159404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76019242..76225826hg38UCSC Ensembl
Innerchr3:76068393..76274977hg19UCSC Ensembl
Innerchr3:76151083..76357667hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38206585
hg19206585
hg18206585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596201, nssv3596199, nssv3596200
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)nsv999868
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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