A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565473



Internal ID20938544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105053998..105054830hg38UCSC Ensembl
chr7:104694445..104695277hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272225
Samples
Known GenesKMT2E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565473
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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