A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009907



Internal ID19099126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35449219..35552716hg38UCSC Ensembl
Innerchr3:35490711..35594208hg19UCSC Ensembl
Innerchr3:35465715..35569212hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38103498
hg19103498
hg18103498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4716n100
Supporting Variantsnssv3589598
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)nsv1009907
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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