A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2739829



Internal ID10323465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97209005..97211954hg38UCSC Ensembl
Outerchr10:98968762..98971711hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382950
hg192950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6906830
SamplesSSM002
Known GenesARHGAP19-SLIT1
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2739829
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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