A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998826



Internal ID19158362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11048220..11139401hg38UCSC Ensembl
Innerchr4:11049844..11141025hg19UCSC Ensembl
Innerchr4:10658942..10750123hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3891182
hg1991182
hg1891182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619753
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)nsv998826
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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