A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011981



Internal ID18754517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:295489..326788hg38UCSC Ensembl
Innerchr4:289278..320577hg19UCSC Ensembl
Innerchr4:279278..310577hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3831300
hg1931300
hg1831300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738102
Samples
Known GenesZNF732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011981
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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