A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014355



Internal ID18756889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56633088..56664453hg38UCSC Ensembl
Innerchr4:57499254..57530619hg19UCSC Ensembl
Innerchr4:57194011..57225376hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3831366
hg1931366
hg1831366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625287
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)nsv1014355
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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