A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708591



Internal ID132257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71802614..71803809hg38UCSC Ensembl
chr16:71836517..71837712hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519209
Supporting Variants
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708591
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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