A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005874



Internal ID18748405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157425..286102hg38UCSC Ensembl
Innerchr4:151220..279891hg19UCSC Ensembl
Innerchr4:141220..269891hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38128678
hg19128672
hg18128672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5074n100
Supporting Variantsnssv3616083
Samples
Known GenesZNF718, 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)nsv1005874
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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