A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006957



Internal ID21916300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99891905..99892033hg38UCSC Ensembl
chr10:101651662..101651790hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586422
Samples
Known GenesDNMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006957
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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