A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066733



Internal ID21975966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155594363..155594363hg38UCSC Ensembl
chr7:155387057..155387057hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066733
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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