A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352085



Internal ID22577754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104320119..104320273hg38UCSC Ensembl
chr10:106079877..106080031hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918682
Supporting Variants
Samples
Known GenesITPRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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