A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800780



Internal ID19164459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129342864..129368819hg38UCSC Ensembl
Innerchr9:132105143..132131098hg19UCSC Ensembl
Innerchr9:131144964..131170919hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3825956
hg1925956
hg1825956
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=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800780
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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