A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010913



Internal ID19100130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..46826hg38UCSC Ensembl
Innerchr4:12269..46822hg19UCSC Ensembl
Innerchr4:2269..36822hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834558
hg1934554
hg1834554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5052n100
Supporting Variantsnssv3737919
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)nsv1010913
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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