A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3697793



Internal ID11717391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1541434..1542211hg38UCSC Ensembl
chr10:1583629..1584406hg19UCSC Ensembl
chr10:1573629..1574406hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38778
hg19778
hg18778
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1416852
Supporting Variants
SamplesHuRef
Known GenesADARB2, ADARB2-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3697793
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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