A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763029



Internal ID20538889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136789067..136789067hg38UCSC Ensembl
chr7:136473814..136473814hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763029
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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