A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860047



Internal ID22043690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136761307..136761307hg38UCSC Ensembl
chr6:137082445..137082445hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257239
Supporting Variants
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860047
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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