A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924571



Internal ID17136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215608288..215614173hg38UCSC Ensembl
chr2:216473011..216478896hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385886
hg195886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436289
Supporting Variants
Samples
Known GenesLINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924571
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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