A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4093615



Internal ID11321573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1593035..1593161hg38UCSC Ensembl
chr10:1635230..1635356hg19UCSC Ensembl
chr10:1625230..1625356hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38127
hg19127
hg18127
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1595476
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4093615
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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