A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6905407



Internal ID9985728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:75383178..75384018hg38UCSC Ensembl
Outerchr9:77998094..77998934hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738567
Supporting Variants
SamplesSSM002
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)essv6905407
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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