A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001881



Internal ID19091098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62410926..62490870hg38UCSC Ensembl
Innerchr4:63276644..63356588hg19UCSC Ensembl
Innerchr4:62959239..63039183hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3879945
hg1979945
hg1879945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739498
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)nsv1001881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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