A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567766



Internal ID20940837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122345452..122346085hg38UCSC Ensembl
chr7:121985506..121986139hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272341
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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