A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6774770



Internal ID10180776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:3643281..3643585hg38UCSC Ensembl
Outerchr7:3682913..3683217hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733875
Supporting Variants
SamplesSSM066
Known GenesSDK1
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)essv6774770
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