A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753429



Internal ID18727675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67524754..67525066hg38UCSC Ensembl
Outerchr17:67524680..67525129hg38UCSC Ensembl
Innerchr17:65520870..65521182hg19UCSC Ensembl
Outerchr17:65520796..65521245hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554682
Supporting Variants
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753429
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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