A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981496



Internal ID55031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47602589..47602625hg38UCSC Ensembl
chr6:47570325..47570361hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553891
Supporting Variants
Samples
Known GenesCD2AP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981496
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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