A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577849



Internal ID21769892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90550383..90550383hg38UCSC Ensembl
chr9:93312665..93312665hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086078
Supporting Variants
Samples
Known GenesLOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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