A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997664



Internal ID18810514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..62032hg38UCSC Ensembl
Innerchr4:12269..61924hg19UCSC Ensembl
Innerchr4:2269..51924hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849764
hg1949656
hg1849656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5054n100
Supporting Variantsnssv3619373
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997664
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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