A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984829



Internal ID21894172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75610759..75610834hg38UCSC Ensembl
chr1:76076444..76076519hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526553
Samples
Known GenesSLC44A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984829
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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