A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910758



Internal ID7940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31953465..31959602hg38UCSC Ensembl
chr2:32178534..32184671hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg386138
hg196138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442111
Supporting Variants
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910758
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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