A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579822



Internal ID21771865
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 StatusS
Merged Variantsnsv6087358
Supporting Variants
Samples
Known GenesMMP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579822
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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