A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909720



Internal ID7252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11659938..11659988hg38UCSC Ensembl
chr2:11800064..11800114hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446079
Supporting Variants
Samples
Known GenesNTSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909720
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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