A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156594



Internal ID22086995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147617313..147758673hg38UCSC Ensembl
Outerchr6:147608823..147759113hg38UCSC Ensembl
Innerchr6:147938449..148079809hg19UCSC Ensembl
Outerchr6:147929959..148080249hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38150291
hg19150291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022699
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156594
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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