A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792578



Internal ID21237916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6798208..6798463hg38UCSC Ensembl
chr12:6907374..6907629hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv56n137
Supporting Variantsnssv13691539
Samples
Known GenesCD4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792578
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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