A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575593



Internal ID20948664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711014..98713745hg38UCSC Ensembl
chr14:99177351..99180082hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382732
hg192732
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238411
Samples
Known GenesC14orf177
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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