A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585165



Internal ID346744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:119250365..119250401hg38UCSC Ensembl
Outerchr9:119246721..119251088hg38UCSC Ensembl
Innerchr9:122012643..122012679hg19UCSC Ensembl
Outerchr9:122008999..122013366hg19UCSC Ensembl
Innerchr9:121052464..121052500hg18UCSC Ensembl
Outerchr9:121048820..121053187hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg384368
hg194368
hg184368
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275135
Supporting Variants
Samples
Known GenesBRINP1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585165
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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