A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538345



Internal ID20911662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94940832..94941315hg38UCSC Ensembl
chr1:95406388..95406871hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253954
Samples
Known GenesLOC729970
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538345
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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