A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557408



Internal ID20930479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105738829..105739500hg38UCSC Ensembl
chr6:106186704..106187375hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6357n223
Supporting Variantsnssv18271075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557408
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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