A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004796



Internal ID19094013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30081570..30321369hg38UCSC Ensembl
Innerchr4:30083192..30322991hg19UCSC Ensembl
Innerchr4:29692290..29932089hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38239800
hg19239800
hg18239800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737772
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)nsv1004796
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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