A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921666



Internal ID15214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158350697..158360892hg38UCSC Ensembl
chr2:159207209..159217404hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3810196
hg1910196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453865
Supporting Variants
Samples
Known GenesCCDC148
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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