A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063820



Internal ID21973053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155367308..155367308hg38UCSC Ensembl
chr7:155160003..155160003hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558561
Samples
Known GenesBLACE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063820
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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