A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925169



Internal ID17531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236381211..236381478hg38UCSC Ensembl
chr2:237289854..237290121hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140079
Supporting Variants
Samples
Known GenesIQCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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