A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004981



Internal ID18747512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25176..59167hg38UCSC Ensembl
Innerchr4:25176..59060hg19UCSC Ensembl
Innerchr4:15176..49060hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3833992
hg1933885
hg1833885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5062n100
Supporting Variantsnssv3615246
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)nsv1004981
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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