A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020241



Internal ID20587281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54968492..54968887hg38UCSC Ensembl
chr14:55435210..55435605hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475952
Supporting Variants
Samples
Known GenesWDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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