A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7752034



Internal ID14524114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2773777..2773778hg38UCSC Ensembl
Innerchr6:2773752..2773803hg38UCSC Ensembl
Outerchr6:2773751..2773804hg38UCSC Ensembl
chr6:2774011..2774012hg19UCSC Ensembl
Innerchr6:2773986..2774037hg19UCSC Ensembl
Outerchr6:2773985..2774038hg19UCSC Ensembl
chr6:2719010..2719011hg18UCSC Ensembl
Innerchr6:2719036..2718985hg18UCSC Ensembl
Outerchr6:2718984..2719037hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38270
hg19270
hg18270
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307182
Supporting Variants
SamplesNA18947
Known GenesWRNIP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7752034
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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