A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6881258



Internal ID9929929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94773903..94774236hg38UCSC Ensembl
Outerchr5:94109608..94109941hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730475
Supporting Variants
SamplesSSM094
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)essv6881258
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