A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913996



Internal ID22689212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44523450..44523521hg38UCSC Ensembl
chr11:44545000..44545071hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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