A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628994



Internal ID21821041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63914028..63920692hg38UCSC Ensembl
chr17:61991388..61998052hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg386665
hg196665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033124
Supporting Variants
Samples
Known GenesGH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628994
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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