A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752831



Internal ID18727077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:7433296..7434228hg38UCSC Ensembl
Outerchr17:7433054..7434433hg38UCSC Ensembl
Innerchr17:7336615..7337547hg19UCSC Ensembl
Outerchr17:7336373..7337752hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752831
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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