A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745153



Internal ID20521158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148387429..148387517hg38UCSC Ensembl
chr6:148708565..148708653hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269627
Samples
Known GenesSASH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745153
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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