A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891729



Internal ID19186125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129342864..129368819hg38UCSC Ensembl
Outerchr9:129342864..129377690hg38UCSC Ensembl
Innerchr9:132105143..132131098hg19UCSC Ensembl
Outerchr9:132105143..132139969hg19UCSC Ensembl
Innerchr9:131144964..131170919hg18UCSC Ensembl
Outerchr9:131144964..131179790hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3834827
hg1934827
hg1834827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784689, essv25800780
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891729
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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