A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269380



Internal ID20836420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151396958..151398016hg38UCSC Ensembl
chr6:151718093..151719151hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269380
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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