A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689231



Internal ID112897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75506401..75506482hg38UCSC Ensembl
chr12:75900181..75900262hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501595
Supporting Variants
Samples
Known GenesKRR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689231
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002659


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