A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156498



Internal ID22086899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40098471..40134977hg38UCSC Ensembl
Outerchr6:40095143..40135568hg38UCSC Ensembl
Innerchr6:40066210..40102716hg19UCSC Ensembl
Outerchr6:40062882..40103307hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3840426
hg1940426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv248n97
Supporting Variantsnssv4018555
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156498
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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