A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440198



Internal ID21097751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127699381..127703216hg38UCSC Ensembl
chr9:130461660..130465495hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383836
hg193836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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