A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543669



Internal ID20916915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238365930..238490330hg38UCSC Ensembl
chr1:238529230..238653630hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38124401
hg19124401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250051
Samples
Known GenesLINC01139
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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