A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568988



Internal ID20942059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99967657..99987029hg38UCSC Ensembl
chr7:99565280..99584652hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3819373
hg1919373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275872
Samples
Known GenesAZGP1, AZGP1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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