A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576130



Internal ID20949201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53118602..53317689hg38UCSC Ensembl
chr14:53585320..53784407hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38199088
hg19199088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237752
Samples
Known GenesDDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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