A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586138



Internal ID20959209
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 StatusM
Merged Variants
Supporting Variantsnssv18218041
Samples
Known GenesKLHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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