A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028323



Internal ID19117541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116260580..116291311hg38UCSC Ensembl
Innerchr5:115596277..115627008hg19UCSC Ensembl
Innerchr5:115624176..115654907hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3830732
hg1930732
hg1830732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5792n100
Supporting Variantsnssv3647185, nssv3647186, nssv3647183, nssv3647182, nssv3647188, nssv3647184, nssv3647187
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028323
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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