A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608172



Internal ID21800219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50828783..50829072hg38UCSC Ensembl
chr12:51222566..51222855hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608172
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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