A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376200



Internal ID22601869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104807605..104854199hg38UCSC Ensembl
chr14:105273942..105320536hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3846595
hg1946595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935781
Supporting Variants
Samples
Known GenesLINC00638
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376200
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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