A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583201



Internal ID20956272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31455295..31455833hg38UCSC Ensembl
chr14:31924501..31925039hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233144
Samples
Known GenesDTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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