A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009105



Internal ID21918448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87200391..87202142hg38UCSC Ensembl
chr7:86829707..86831458hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381752
hg191752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575340
Samples
Known GenesTMEM243
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009105
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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