A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441113



Internal ID21098666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128408486..128409502hg38UCSC Ensembl
chr9:131170765..131171781hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176873, nssv18236987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441113
Frequency
Sample Size19652
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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