A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859915



Internal ID22043558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155237226..155237226hg38UCSC Ensembl
chr6:155558360..155558360hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257385
Supporting Variants
Samples
Known GenesTIAM2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859915
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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