A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010090



Internal ID21919433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100276329..100276418hg38UCSC Ensembl
chr10:102036086..102036175hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579030
Samples
Known GenesBLOC1S2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010090
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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