A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744999



Internal ID18372559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48709133..48709426hg38UCSC Ensembl
Outerchr10:48709073..48709469hg38UCSC Ensembl
Innerchr10:49917178..49917471hg19UCSC Ensembl
Outerchr10:49917118..49917514hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546252
Supporting Variants
Samples
Known GenesWDFY4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744999
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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