A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474801



Internal ID21132354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35395232..35400217hg38UCSC Ensembl
chr11:35416779..35421764hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384986
hg194986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990906
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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