A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616770



Internal ID21808817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71212974..71217872hg38UCSC Ensembl
chr14:71679691..71684589hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384899
hg194899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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