A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839334



Internal ID22022977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140908987..140908987hg38UCSC Ensembl
chr7:140608787..140608787hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239844
Supporting Variants
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839334
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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