A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735403



Internal ID20511345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77869865..77869917hg38UCSC Ensembl
chr1:78335550..78335602hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259158
Samples
Known GenesFAM73A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735403
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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