A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784689



Internal ID19179172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129342864..129377690hg38UCSC Ensembl
Innerchr9:132105143..132139969hg19UCSC Ensembl
Innerchr9:131144964..131179790hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3834827
hg1934827
hg1834827
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891729
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784689
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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