A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634579



Internal ID21826626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34934418..34934514hg38UCSC Ensembl
chr20:33522221..33522317hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053195
Supporting Variants
Samples
Known GenesGSS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634579
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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