A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915364



Internal ID10980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97207905..97209771hg38UCSC Ensembl
chr2:97873642..97875508hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436097
Supporting Variants
Samples
Known GenesANKRD36
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915364
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.107623


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