A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563634



Internal ID7036394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76362158..76370420hg38UCSC Ensembl
Outerchr17:74358239..74366501hg19UCSC Ensembl
Outerchr17:71869834..71878096hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg388263
hg198263
hg188263
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994582
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563634
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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