A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559027



Internal ID20932098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80470941..80471272hg38UCSC Ensembl
chr7:80100257..80100588hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276692
Samples
Known GenesGNAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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