A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004364



Internal ID7069461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:96845176..96852739hg38UCSC Ensembl
Outerchr7:96474488..96482051hg19UCSC Ensembl
Outerchr7:96312424..96319987hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387564
hg197564
hg187564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563963
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004364
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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