A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568989



Internal ID21761032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19939929..19940135hg38UCSC Ensembl
chr6:19940160..19940366hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568989
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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