A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537617



Internal ID20910953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52891950..52892429hg38UCSC Ensembl
chr1:53357622..53358101hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249761
Samples
Known GenesZYG11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537617
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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