A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566018



Internal ID21758061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40037296..40160445hg38UCSC Ensembl
chr7:40076895..40200044hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38123150
hg19123150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006062
Supporting Variants
Samples
Known GenesC7orf10, CDK13, MPLKIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566018
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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