A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736077



Internal ID20512022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35372445..35373744hg38UCSC Ensembl
chr9:35372442..35373741hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291026
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736077
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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