A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604524



Internal ID21796571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8879399..8880275hg38UCSC Ensembl
chr12:9031995..9032871hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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