A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567222



Internal ID20940293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122238556..122284886hg38UCSC Ensembl
chr7:121878610..121924940hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3846331
hg1946331
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567222
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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