A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591098



Internal ID20964169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71608615..71609592hg38UCSC Ensembl
chr14:72075332..72076309hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238608
Samples
Known GenesSIPA1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591098
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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