A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274829



Internal ID20841869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85649755..85650408hg38UCSC Ensembl
chr6:86359473..86360126hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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