A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998791



Internal ID19158327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38462872..38540841hg38UCSC Ensembl
Innerchr4:38464493..38542462hg19UCSC Ensembl
Innerchr4:38140888..38218857hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3877970
hg1977970
hg1877970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5192n100
Supporting Variantsnssv3625032
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)nsv998791
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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