A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895116



Internal ID22670193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10681224..10681399hg38UCSC Ensembl
chr5:10681336..10681511hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414343
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895116
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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