A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16917015



Internal ID12081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97192916..97192916hg38UCSC Ensembl
chr2:97858653..97858653hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381871
hg191871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548124
Supporting Variants
Samples
Known GenesANKRD36
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16917015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.025448


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