A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811091



Internal ID21256429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123236806..123237328hg38UCSC Ensembl
chr5:122572500..122573022hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811091
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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