A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377085



Internal ID22434955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98737266..98742803hg38UCSC Ensembl
chr14:99203603..99209140hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385538
hg195538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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