A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619526



Internal ID6659712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9798117..9823348hg38UCSC Ensembl
Innerchr9:9798137..9823329hg38UCSC Ensembl
Outerchr9:9798098..9823368hg38UCSC Ensembl
chr9:9798117..9823348hg19UCSC Ensembl
Innerchr9:9798137..9823329hg19UCSC Ensembl
Outerchr9:9798098..9823368hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3825232
hg1925232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1439e214
Supporting Variantsessv13396623, essv13396621, essv13396622
SamplesNA20802, HG01524, NA11840
Known GenesPTPRD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619526
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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