A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391365



Internal ID22449235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100409559..100409615hg38UCSC Ensembl
chr2:101026021..101026077hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885568
Supporting Variants
Samples
Known GenesCHST10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391365
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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