A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574669



Internal ID6699365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1409637..1410081hg38UCSC Ensembl
chr10:1451832..1452276hg19UCSC Ensembl
chr10:1441832..1442276hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38445
hg19445
hg18445
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009491
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574669
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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