A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010599



Internal ID19099816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:41756786..41795382hg38UCSC Ensembl
Innerchr4:41758803..41797399hg19UCSC Ensembl
Innerchr4:41453560..41492156hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3838597
hg1938597
hg1838597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5196n100
Supporting Variantsnssv3625047
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)nsv1010599
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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