A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999966



Internal ID18812816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..61871hg38UCSC Ensembl
Innerchr4:12269..61763hg19UCSC Ensembl
Innerchr4:2269..51763hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849603
hg1949495
hg1849495
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5055n100
Supporting Variantsnssv3619370, nssv3619372, nssv3619371
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)nsv999966
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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