A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021856



Internal ID20588896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77683579..77684216hg38UCSC Ensembl
chr14:78149922..78150559hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476777
Supporting Variants
Samples
Known GenesALKBH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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