A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998311



Internal ID18811161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2979888..3010996hg38UCSC Ensembl
Innerchr4:2981615..3012723hg19UCSC Ensembl
Innerchr4:2951413..2982521hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3831109
hg1931109
hg1831109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616114
Samples
Known GenesGRK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998311
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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