A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011335



Internal ID19100552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:41756786..41788583hg38UCSC Ensembl
Innerchr4:41758803..41790600hg19UCSC Ensembl
Innerchr4:41453560..41485357hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3831798
hg1931798
hg1831798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5196n100
Supporting Variantsnssv3625046
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)nsv1011335
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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