A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv263n137



Internal ID22812883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70516302..70516405hg38UCSC Ensembl
chr4:71382019..71382122hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2809610, nsv2810705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv263n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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