A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999861



Internal ID18812711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101654958..102009405hg38UCSC Ensembl
Innerchr4:102576115..102930562hg19UCSC Ensembl
Innerchr4:102795138..103149585hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38354448
hg19354448
hg18354448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631013
Samples
Known GenesBANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999861
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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