A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597592



Internal ID21789635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18855866..18856050hg38UCSC Ensembl
chr12:19008800..19008984hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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