A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582156



Internal ID20955227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91441021..91441606hg38UCSC Ensembl
chr14:91907365..91907950hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582156
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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