A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6691873



Internal ID10105090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:96709006..96709372hg38UCSC Ensembl
Outerchr14:97175343..97175709hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749073, esv2749069, esv2749071, esv2749066, esv2749064
Supporting Variants
SamplesSSM036
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)essv6691873
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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