A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843458



Internal ID22027101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102529830..102529830hg38UCSC Ensembl
chr11:102400561..102400561hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258255
Supporting Variants
Samples
Known GenesMMP7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843458
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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