A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019587



Internal ID18762122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144845376..144957167hg38UCSC Ensembl
Innerchr4:145766528..145878319hg19UCSC Ensembl
Innerchr4:145985978..146097769hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38111792
hg19111792
hg18111792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744262
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)nsv1019587
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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