A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627206



Internal ID21819253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81119713..81119798hg38UCSC Ensembl
chr17:79093513..79093598hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025690
Supporting Variants
Samples
Known GenesAATK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627206
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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