A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606297



Internal ID21798344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96434136..96435777hg38UCSC Ensembl
chr12:96827914..96829555hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381642
hg191642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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