A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539644



Internal ID20912940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13491455..13492581hg38UCSC Ensembl
chr1:13817907..13819033hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249946
Samples
Known GenesLRRC38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539644
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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