A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001899



Internal ID18744430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..523947hg38UCSC Ensembl
Innerchr4:68809..517736hg19UCSC Ensembl
Innerchr4:58809..507736hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38455031
hg19448928
hg18448928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738092
Samples
Known GenesABCA11P, PIGG, ZNF141, ZNF595, ZNF718, ZNF721, ZNF732, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001899
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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