A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574981



Internal ID20948052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94718017..94943192hg38UCSC Ensembl
chr6:95427735..95652910hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38225176
hg19225176
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574981
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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