A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010803



Internal ID19100020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82659093..82717637hg38UCSC Ensembl
Innerchr3:82708244..82766788hg19UCSC Ensembl
Innerchr3:82790934..82849478hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3858545
hg1958545
hg1858545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4800n100
Supporting Variantsnssv3596241
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)nsv1010803
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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