A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563705



Internal ID7036465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98024269..98034306hg38UCSC Ensembl
Outerchr7:97653581..97663618hg19UCSC Ensembl
Outerchr7:97491517..97501554hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3810038
hg1910038
hg1810038
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000353
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563705
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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