A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087358



Internal ID21996591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125766494..125766494hg38UCSC Ensembl
chr10:127455063..127455063hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579822
Samples
Known GenesMMP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087358
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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