A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857798



Internal ID22041441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94806276..94806276hg38UCSC Ensembl
chr5:94141981..94141981hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244550
Supporting Variants
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857798
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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