A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744892



Internal ID18719138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34395560..34395837hg38UCSC Ensembl
Outerchr10:34395504..34395908hg38UCSC Ensembl
Innerchr10:34684488..34684765hg19UCSC Ensembl
Outerchr10:34684432..34684836hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546145
Supporting Variants
Samples
Known GenesPARD3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744892
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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