A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595480



Internal ID20968551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74052538..74053236hg38UCSC Ensembl
chr14:74519241..74519939hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237242
Samples
Known GenesCCDC176
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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