A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999242



Internal ID7082077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:35355002..35366095hg38UCSC Ensembl
Outerchr7:35394612..35405705hg19UCSC Ensembl
Outerchr7:35361137..35372230hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3811094
hg1911094
hg1811094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564957
SamplesHuRef
Known GenesLOC401324
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999242
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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