A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749655



Internal ID20525687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51203211..51203478hg38UCSC Ensembl
chr7:51270908..51271175hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272694
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749655
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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