A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891565



Internal ID18839275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9729134..10077180hg38UCSC Ensembl
Outerchr9:9729134..10077180hg38UCSC Ensembl
Innerchr9:9729134..10077180hg19UCSC Ensembl
Outerchr9:9729134..10077180hg19UCSC Ensembl
Innerchr9:9719134..10067180hg18UCSC Ensembl
Outerchr9:9719134..10067180hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38348047
hg19348047
hg18348047
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788011
Samples
Known GenesPTPRD
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891565
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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