A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546101



Internal ID20919320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67310196..67310749hg38UCSC Ensembl
chr1:67775879..67776432hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251267
Samples
Known GenesIL12RB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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