A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6872079



Internal ID9921667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:232326583..232440017hg38UCSC Ensembl
Outerchr2:233191293..233304727hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38113435
hg19113435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2721624
Supporting Variants
SamplesSSM091
Known GenesALPP, ALPPL2, DIS3L2, ECEL1P2
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)essv6872079
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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