A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640474



Internal ID6680561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36564700..36908342hg38UCSC Ensembl
chr17:34920539..35265627hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38343643
hg19345089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15666457, essv15666456
SamplesNA20359, NA20362
Known GenesDHRS11, GGNBP2, MRM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640474
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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