A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6757955



Internal ID9818807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133760093..133761094hg38UCSC Ensembl
Outerchr9:136625215..136626216hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739138, esv2739179
Supporting Variants
SamplesSSM059
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)essv6757955
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer