A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377453



Internal ID22435323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68116447..68116522hg38UCSC Ensembl
chr17:66112588..66112663hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944904
Supporting Variants
Samples
Known GenesLINC00674
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377453
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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