A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568589



Internal ID20941660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5998097..5998751hg38UCSC Ensembl
chr7:6037728..6038382hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6554n223
Supporting Variantsnssv18275432
Samples
Known GenesPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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