A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218041



Internal ID20785081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49746684..49747957hg38UCSC Ensembl
chr14:50213402..50214675hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586138
Supporting Variants
Samples
Known GenesKLHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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