A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073692



Internal ID21982925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31852984..31852984hg38UCSC Ensembl
chr7:31892598..31892598hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559977
Samples
Known GenesPDE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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