A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025544



Internal ID21934887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35402779..35402943hg38UCSC Ensembl
chr11:35424326..35424490hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589845
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025544
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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