A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1315028



Internal ID12131464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97275116..97277650hg38UCSC Ensembl
chr10:99034873..99037407hg19UCSC Ensembl
chr10:99024863..99027397hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382535
hg192535
hg182535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4127672
SamplesHuRef
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1315028
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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