A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071802



Internal ID21981035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135857880..135857880hg38UCSC Ensembl
chr6:136179018..136179018hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571950
Samples
Known GenesPDE7B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071802
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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