A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553959



Internal ID18755035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:841382..841686hg38UCSC Ensembl
Outerchr17:841370..841691hg38UCSC Ensembl
Innerchr17:744622..744926hg19UCSC Ensembl
Outerchr17:744610..744931hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752706
Samples
Known GenesNXN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553959
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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