A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020197



Internal ID19109416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101659168..101949666hg38UCSC Ensembl
Innerchr5:100994872..101285370hg19UCSC Ensembl
Innerchr5:101022771..101313269hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38290499
hg19290499
hg18290499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5742n100
Supporting Variantsnssv3748296, nssv3645828
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)nsv1020197
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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