A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156595



Internal ID22086996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148731267..148736360hg38UCSC Ensembl
Outerchr6:148728633..148750828hg38UCSC Ensembl
Innerchr6:149052403..149057496hg19UCSC Ensembl
Outerchr6:149049769..149071964hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3822196
hg1922196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022700
Samples
Known GenesUST
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156595
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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