A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557696



Internal ID21882051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99650200..99650256hg38UCSC Ensembl
chr6:100098076..100098132hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557696
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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