A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552422



Internal ID20925549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24208763..24209669hg38UCSC Ensembl
chr1:24535253..24536159hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250156
Samples
Known GenesLOC284632
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552422
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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