A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007539



Internal ID19096758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57273231..57701228hg38UCSC Ensembl
Innerchr4:58139397..58567394hg19UCSC Ensembl
Innerchr4:57834154..58262151hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38427998
hg19427998
hg18427998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5218n100
Supporting Variantsnssv3626502
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007539
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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