A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066705



Internal ID21975938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137852973..137852973hg38UCSC Ensembl
chr7:137537719..137537719hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066705
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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