A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730081



Internal ID153747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213190609..213191385hg38UCSC Ensembl
chr2:214055333..214056109hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730081
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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