A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565495



Internal ID21757460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140909964..140909964hg38UCSC Ensembl
chr7:140609764..140609764hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074503
Supporting Variants
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565495
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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