A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582108



Internal ID20955179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61732021..61733247hg38UCSC Ensembl
chr14:62198739..62199965hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237181
Samples
Known GenesHIF1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582108
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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