A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455291



Internal ID21112844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114540265..114541627hg38UCSC Ensembl
chr9:117302545..117303907hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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