A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021579



Internal ID20588620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88022458..88100088hg38UCSC Ensembl
chr14:88488802..88566432hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3877631
hg1977631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477641
Supporting Variants
Samples
Known GenesLINC01146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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