A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749604



Internal ID20525636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59696988..59697116hg38UCSC Ensembl
chr10:61456746..61456874hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260057
Samples
Known GenesSLC16A9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749604
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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