A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738780



Internal ID9973121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93080099..93080259hg38UCSC Ensembl
Outerchr9:95842381..95842541hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6976283
SamplesSSM029
Known GenesSUSD3
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)esv2738780
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