A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275059



Internal ID1279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25348426..25351016hg38UCSC Ensembl
Outerchr6:25346757..25351035hg38UCSC Ensembl
Innerchr6:25348654..25351244hg19UCSC Ensembl
Outerchr6:25346985..25351263hg19UCSC Ensembl
Innerchr6:25456633..25459223hg18UCSC Ensembl
Outerchr6:25454964..25459242hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg384279
hg194279
hg184279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585178
Samples
Known GenesLRRC16A
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275059
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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