A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542282



Internal ID20915546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35233348..35234865hg38UCSC Ensembl
chr1:35698949..35700466hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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