A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6875479



Internal ID10271414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3499152..3499548hg38UCSC Ensembl
Outerchr5:3499266..3499662hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729641
Supporting Variants
SamplesSSM092
Known GenesLINC01019, LOC102467075
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)essv6875479
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