A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006940



Internal ID19096158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34459992..34568760hg38UCSC Ensembl
Innerchr4:34461614..34570382hg19UCSC Ensembl
Innerchr4:34138009..34246777hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38108769
hg19108769
hg18108769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737778
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)nsv1006940
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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