A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914665



Internal ID10525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71701554..71701611hg38UCSC Ensembl
chr2:71928684..71928741hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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