A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543827



Internal ID20917068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38760533..38761285hg38UCSC Ensembl
chr1:39226205..39226957hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543827
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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