A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547362



Internal ID20920565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32120237..32122140hg38UCSC Ensembl
chr1:32585838..32587741hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381904
hg191904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250815
Samples
Known GenesKPNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547362
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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