A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539301



Internal ID20912602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32777164..32777468hg38UCSC Ensembl
chr1:33242765..33243069hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250872
Samples
Known GenesYARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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