A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6712722



Internal ID9778537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35150752..35151134hg38UCSC Ensembl
Outerchr10:35439680..35440062hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735350, esv2735328
Supporting Variants
SamplesSSM042
Known GenesCREM
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)essv6712722
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer