A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587327



Internal ID21779370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122470474..122470474hg38UCSC Ensembl
chr10:124229990..124229990hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094854
Supporting Variants
Samples
Known GenesHTRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587327
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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