A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451970



Internal ID21109523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31253708..31628668hg38UCSC Ensembl
chr11:31275255..31650215hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38374961
hg19374961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989635
Samples
Known GenesDCDC1, DNAJC24, ELP4, IMMP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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