A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038809



Internal ID93617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122503265..122504236hg38UCSC Ensembl
chr10:124262781..124263752hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504605
Supporting Variants
Samples
Known GenesHTRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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