A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023043



Internal ID19112260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99986588..100110472hg38UCSC Ensembl
Innerchr5:99322292..99446176hg19UCSC Ensembl
Innerchr5:99350191..99474075hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38123885
hg19123885
hg18123885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5733n100
Supporting Variantsnssv3748283, nssv3638081, nssv3638079, nssv3638080, nssv3638082, nssv3748285, nssv3638083, nssv3748284
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)nsv1023043
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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