A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739565



Internal ID20515539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73045198..73045325hg38UCSC Ensembl
chr9:75660114..75660241hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739565
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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