A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004375



Internal ID21913718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44112327..44112541hg38UCSC Ensembl
chr10:44607775..44607989hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004375
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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