A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598595



Internal ID21790640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56907732..56908839hg38UCSC Ensembl
chr12:57301516..57302623hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598595
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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