A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6720009



Internal ID9650462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:207502415..207675480hg38UCSC Ensembl
Outerchr1:207675760..207848825hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38173066
hg19173066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722106
Supporting Variants
SamplesSSM007
Known GenesCR1, CR1L
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)essv6720009
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