A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584039



Internal ID21776082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96209126..96209126hg38UCSC Ensembl
chr10:97968882..97968882hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089275
Supporting Variants
Samples
Known GenesBLNK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584039
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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