A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6922189



Internal ID9688213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:178436474..178443260hg38UCSC Ensembl
Outerchr2:179301201..179307987hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg386787
hg196787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2721191
Supporting Variants
SamplesSSM018
Known GenesMIR548N, PRKRA
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)essv6922189
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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