A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603751



Internal ID21795798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77196698..77201589hg38UCSC Ensembl
chr12:77590478..77595369hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg384892
hg194892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603751
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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