A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570873



Internal ID20943944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24470781..24471379hg38UCSC Ensembl
chr6:24471009..24471607hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270862
Samples
Known GenesGPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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