A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031406



Internal ID19120628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12231185..12305730hg38UCSC Ensembl
Innerchr5:12231297..12305842hg19UCSC Ensembl
Innerchr5:12284297..12358842hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3874546
hg1974546
hg1874546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638203
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)nsv1031406
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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