A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012174



Internal ID21921517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131609292..131609530hg38UCSC Ensembl
chr6:131930432..131930670hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567695
Samples
Known GenesMED23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012174
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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