A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593026



Internal ID21785069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6797534..6802501hg38UCSC Ensembl
chr10:6839496..6844463hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384968
hg194968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007537
Supporting Variants
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593026
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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