A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003170



Internal ID6715305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97273649..97277902hg38UCSC Ensembl
Outerchr10:99033406..99037659hg19UCSC Ensembl
Outerchr10:99023396..99027649hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg384254
hg194254
hg184254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563832
SamplesHuRef
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003170
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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