A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573624



Internal ID20946695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72446419..72448531hg38UCSC Ensembl
chr9:75061335..75063447hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382113
hg192113
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7828n223
Supporting Variantsnssv18280922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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