A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032364



Internal ID21941707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29558341..29558431hg38UCSC Ensembl
chr13:30132478..30132568hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602047
Samples
Known GenesSLC7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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