A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571507



Internal ID20944578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37514036..37518167hg38UCSC Ensembl
chr8:37371554..37375685hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg384132
hg194132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571507
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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