A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352086



Internal ID22577755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100734580..100734654hg38UCSC Ensembl
chr10:102494337..102494411hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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