A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013595



Internal ID18756127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4062785..4195504hg38UCSC Ensembl
Innerchr3:4104469..4237188hg19UCSC Ensembl
Innerchr3:4079469..4212188hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38132720
hg19132720
hg18132720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4644n100
Supporting Variantsnssv3590441
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)nsv1013595
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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