A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610340



Internal ID21802387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8787085..8794583hg38UCSC Ensembl
chr12:8939681..8947179hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg387499
hg197499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033410
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610340
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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