A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454627



Internal ID21112180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128799883..128801073hg38UCSC Ensembl
chr9:131562162..131563352hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176914
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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