A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6670829



Internal ID9740066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:95207919..95207970hg38UCSC Ensembl
Outerchr5:94543623..94543674hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730477
Supporting Variants
SamplesSSM031
Known GenesMCTP1
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)essv6670829
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