A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602893



Internal ID21794940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2008327..2008382hg38UCSC Ensembl
chr12:2117493..2117548hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602893
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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