A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035267



Internal ID91247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71711915..71712007hg38UCSC Ensembl
chr10:73471672..73471764hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476806
Supporting Variants
Samples
Known GenesC10orf105, CDH23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035267
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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