A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2721705



Internal ID10305341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:236379541..236379820hg38UCSC Ensembl
Outerchr2:237288184..237288463hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6906615, essv6848165, essv6864556, essv6686550, essv6889430
SamplesSSM011, SSM097, SSM089, SSM035, SSM014
Known GenesIQCA1
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)esv2721705
Frequency
Sample Size96
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer