A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008429



Internal ID19097647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82040499..82461385hg38UCSC Ensembl
Innerchr3:82089650..82510536hg19UCSC Ensembl
Innerchr3:82172340..82593226hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38420887
hg19420887
hg18420887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596239, nssv3596238
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)nsv1008429
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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