A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474621



Internal ID21132174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62852425..62852807hg38UCSC Ensembl
chr11:62619897..62620279hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993236
Samples
Known GenesSNHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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