A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615897



Internal ID6656095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:2940539..3065852hg38UCSC Ensembl
chr8:2798061..2923374hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38125314
hg19125314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1357e214
Supporting Variantsessv13070076, essv13070078, essv13070077, essv13070075
SamplesNA19058, NA19448, NA19455, HG03136
Known GenesCSMD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615897
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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