A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593636



Internal ID20966707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70122788..70123791hg38UCSC Ensembl
chr14:70589505..70590508hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238569
Samples
Known GenesSLC8A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593636
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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