A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765443



Internal ID20541303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73588486..73588486hg38UCSC Ensembl
chr7:73002816..73002816hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765443
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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