A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278634



Internal ID20845674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70639225..70639784hg38UCSC Ensembl
chr8:71551460..71552019hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566514
Supporting Variants
Samples
Known GenesLACTB2, LOC286190
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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