A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922558



Internal ID15803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176331906..176334608hg38UCSC Ensembl
chr2:177196634..177199336hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435309
Supporting Variants
Samples
Known GenesMTX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922558
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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