A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575396



Internal ID20948467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94681190..94682401hg38UCSC Ensembl
chr8:95693418..95694629hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279109
Samples
Known GenesESRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575396
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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