A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451647



Internal ID21109200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135993028..136048401hg38UCSC Ensembl
chr9:138884874..138940247hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3855374
hg1955374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176034
Samples
Known GenesNACC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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