A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032913



Internal ID89639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56275910..56400064hg38UCSC Ensembl
chr10:58035671..58159825hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38124155
hg19124155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490706
Supporting Variants
Samples
Known GenesZWINT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032913
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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