A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563388



Internal ID20936459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98384121..98384669hg38UCSC Ensembl
chr7:98013433..98013981hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275809
Samples
Known GenesBAIAP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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