A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010350



Internal ID19099567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32063140..32095507hg38UCSC Ensembl
Innerchr3:32104632..32136999hg19UCSC Ensembl
Innerchr3:32079636..32112003hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3832368
hg1932368
hg1832368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589584
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)nsv1010350
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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