A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587712



Internal ID20960783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101467474..101469392hg38UCSC Ensembl
chr14:101933811..101935729hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381919
hg191919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587712
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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