A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv56n137



Internal ID22812676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6798208..6798474hg38UCSC Ensembl
chr12:6907374..6907640hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2792578, nsv2792490
Samples
Known GenesCD4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv56n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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