A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538321



Internal ID20911638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52818872..52819693hg38UCSC Ensembl
chr1:53284544..53285365hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249752
Samples
Known GenesZYG11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538321
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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