A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv76e201



Internal ID20124963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1408978..1409511hg38UCSC Ensembl
chr10:1451173..1451706hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2729773, esv2729762
SamplesSSM027, SSM086, SSM071, SSM023, SSM079, SSM068, SSM026
Known GenesADARB2
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv76e201
Frequency
Sample Size96
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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