A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006496



Internal ID21915839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91139100..91139153hg38UCSC Ensembl
chr7:90768415..90768468hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575968
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006496
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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