A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735618



Internal ID20511562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32694029..32694104hg38UCSC Ensembl
chr9:32694027..32694102hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735618
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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