A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6968963



Internal ID9729414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:177593111..177593441hg38UCSC Ensembl
Outerchr4:178514265..178514595hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2728790, esv2728772
Supporting Variants
SamplesSSM028
Known Genes
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)essv6968963
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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