A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627734



Internal ID21819781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34372608..34372679hg38UCSC Ensembl
chr20:32960414..32960485hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049129
Supporting Variants
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627734
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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