A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748073



Internal ID20524097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19068329..19068448hg38UCSC Ensembl
chr9:19068327..19068446hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273863
Samples
Known GenesHAUS6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748073
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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