A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016557



Internal ID19105776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58014541..58037116hg38UCSC Ensembl
Innerchr5:57310368..57332943hg19UCSC Ensembl
Innerchr5:57346125..57368700hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3822576
hg1922576
hg1822576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5673n100
Supporting Variantsnssv3642163
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)nsv1016557
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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