A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811399



Internal ID21256737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55105974..55106228hg38UCSC Ensembl
chr5:54401802..54402056hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv289n137
Supporting Variantsnssv13700159
Samples
Known GenesGZMA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811399
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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