A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352168



Internal ID22577837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121200571..121200635hg38UCSC Ensembl
chr10:122960085..122960149hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352168
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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