A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541704



Internal ID20914986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27836537..27837767hg38UCSC Ensembl
chr1:28163048..28164278hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249053
Samples
Known GenesPPP1R8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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