A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3377976



Internal ID14878244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87936200..87936200hg38UCSC Ensembl
Innerchr7:87936199..87936201hg38UCSC Ensembl
Outerchr7:87936140..87936250hg38UCSC Ensembl
chr7:87565515..87565515hg19UCSC Ensembl
Innerchr7:87565514..87565516hg19UCSC Ensembl
Outerchr7:87565455..87565565hg19UCSC Ensembl
chr7:87403451..87403451hg18UCSC Ensembl
Innerchr7:87403452..87403450hg18UCSC Ensembl
Outerchr7:87403391..87403501hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8841512
SamplesNA19240
Known GenesADAM22
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3377976
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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