A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001714



Internal ID7066838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:76726127..76751921hg38UCSC Ensembl
Outerchr6:77435844..77461638hg19UCSC Ensembl
Outerchr6:77492563..77518357hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3825795
hg1925795
hg1825795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563541
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001714
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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