A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999590



Internal ID19159127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:435303..488008hg38UCSC Ensembl
Innerchr4:429092..481797hg19UCSC Ensembl
Innerchr4:419092..471797hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3852706
hg1952706
hg1852706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5078n100
Supporting Variantsnssv3738104
Samples
Known GenesABCA11P, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999590
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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