A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549791



Internal ID20883390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67309554..67310989hg38UCSC Ensembl
chr1:67775237..67776672hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251266
Samples
Known GenesIL12RB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549791
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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