A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021187



Internal ID20588227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76492403..76493352hg38UCSC Ensembl
chr14:76958746..76959695hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490450
Supporting Variants
Samples
Known GenesESRRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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