A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558696



Internal ID21883051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81433852..81433981hg38UCSC Ensembl
chr6:82143569..82143698hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558696
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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