A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086337



Internal ID21995570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100276375..100276375hg38UCSC Ensembl
chr10:102036132..102036132hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583363
Samples
Known GenesBLOC1S2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086337
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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