A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004948



Internal ID21914291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128806840..128806898hg38UCSC Ensembl
chr9:131569119..131569177hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586127
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004948
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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