A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274084



Internal ID20841124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73424235..73424912hg38UCSC Ensembl
chr6:74133958..74134635hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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