A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022886



Internal ID19112103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:128674348..128705163hg38UCSC Ensembl
Innerchr5:128010041..128040856hg19UCSC Ensembl
Innerchr5:128037940..128068755hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3830816
hg1930816
hg1830816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746636
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)nsv1022886
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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