A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922607



Internal ID15839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178986292..179022477hg38UCSC Ensembl
chr2:179851019..179887204hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3836186
hg1936186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452838
Supporting Variants
Samples
Known GenesCCDC141
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922607
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001874


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