A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577606



Internal ID20950677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74720134..74723104hg38UCSC Ensembl
chr10:76479892..76482862hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382971
hg192971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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