A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909752



Internal ID7271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11981511..11992283hg38UCSC Ensembl
chr2:12121637..12132409hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3810773
hg1910773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909752
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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