A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456613



Internal ID22514491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54986339..54990397hg38UCSC Ensembl
chr14:55453057..55457115hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg384059
hg194059
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859721
Supporting Variants
Samples
Known GenesWDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456613
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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