A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7129802



Internal ID10408084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165839809..165840123hg38UCSC Ensembl
Outerchr6:166253297..166253611hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2860235
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7129802
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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