A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459175



Internal ID21116728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35341757..35342034hg38UCSC Ensembl
chr11:35363304..35363581hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990902
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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