A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988957



Internal ID60063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148999593..148999812hg38UCSC Ensembl
chr6:149320729..149320948hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467260
Supporting Variants
Samples
Known GenesUST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988957
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.023884


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