A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472628



Internal ID21130181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83648022..83648506hg38UCSC Ensembl
chr11:83359065..83359549hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994378
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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