A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv289n137



Internal ID22812909
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 Variants
Supporting Variantsnsv2812124, nsv2811399
Samples
Known GenesGZMA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv289n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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