A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752704



Internal ID18726950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:820603..821493hg38UCSC Ensembl
Outerchr17:820401..821725hg38UCSC Ensembl
Innerchr17:723843..724733hg19UCSC Ensembl
Outerchr17:723641..724965hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553957
Supporting Variants
Samples
Known GenesNXN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752704
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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