A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011442



Internal ID21920785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135966608..135999302hg38UCSC Ensembl
chr5:135302297..135334991hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3832695
hg1932695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011442
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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