A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000406



Internal ID18742937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56633088..56678324hg38UCSC Ensembl
Innerchr4:57499254..57544490hg19UCSC Ensembl
Innerchr4:57194011..57239247hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3845237
hg1945237
hg1845237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625288
Samples
Known GenesHOPX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000406
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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