A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998800



Internal ID19158336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10928006..10979667hg38UCSC Ensembl
Innerchr4:10929630..10981291hg19UCSC Ensembl
Innerchr4:10538728..10590389hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3851662
hg1951662
hg1851662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737696
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)nsv998800
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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