A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014322



Internal ID18756856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:21335..66074hg38UCSC Ensembl
Innerchr4:21335..65966hg19UCSC Ensembl
Innerchr4:11335..55966hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3844740
hg1944632
hg1844632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5062n100
Supporting Variantsnssv3615236
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)nsv1014322
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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