A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615072



Internal ID21807119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76755553..76762704hg38UCSC Ensembl
chr14:77221896..77229047hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387152
hg197152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023765
Supporting Variants
Samples
Known GenesVASH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615072
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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