A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278700



Internal ID20845740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74046095..74047070hg38UCSC Ensembl
chr8:74958330..74959305hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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