A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258254



Internal ID22062864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102525484..102525484hg38UCSC Ensembl
chr11:102396215..102396215hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843457
Samples
Known GenesMMP7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258254
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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