A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560604



Internal ID20933675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24457019..24457403hg38UCSC Ensembl
chr6:24457247..24457631hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270860
Samples
Known GenesGPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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