A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007500



Internal ID19096719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166987368..167086514hg38UCSC Ensembl
Innerchr3:166705156..166804302hg19UCSC Ensembl
Innerchr3:168187850..168286996hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3899147
hg1999147
hg1899147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3612696
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)nsv1007500
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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