A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557239



Internal ID20930310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117515132..117516077hg38UCSC Ensembl
chr6:117836295..117837240hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268592
Samples
Known GenesDCBLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557239
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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