A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013921



Internal ID21923264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2972231..2972360hg38UCSC Ensembl
chr6:2972465..2972594hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013921
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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