A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574182



Internal ID6698878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97275110..97277643hg38UCSC Ensembl
chr10:99034867..99037400hg19UCSC Ensembl
chr10:99024857..99027390hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382534
hg192534
hg182534
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001501
Supporting Variants
SamplesHuRef
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574182
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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