A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562762



Internal ID20935833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73925005..73927038hg38UCSC Ensembl
chr9:76539921..76541954hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280953
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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