A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017092



Internal ID19106309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:144993779..145031775hg38UCSC Ensembl
Innerchr5:144373342..144411338hg19UCSC Ensembl
Innerchr5:144353535..144391531hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3837997
hg1937997
hg1837997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5815n100
Supporting Variantsnssv3648155
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)nsv1017092
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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