A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615895



Internal ID6656093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:2895602..3063047hg38UCSC Ensembl
chr8:2753124..2920569hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38167446
hg19167446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1357e214
Supporting Variantsessv13070073
SamplesHG03136
Known GenesCSMD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615895
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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