A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7736898



Internal ID12764698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56826166..56826186hg38UCSC Ensembl
Outerchr18:56825966..56826386hg38UCSC Ensembl
Innerchr18:54493397..54493417hg19UCSC Ensembl
Outerchr18:54493197..54493617hg19UCSC Ensembl
Innerchr18:52644395..52644415hg18UCSC Ensembl
Outerchr18:52644195..52644615hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38421
hg19421
hg18421
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302922
Supporting Variants
SamplesNA10851
Known GenesWDR7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7736898
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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