A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005549



Internal ID21914892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91409427..91409503hg38UCSC Ensembl
chr10:93169184..93169260hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594889
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005549
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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