A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587234



Internal ID6711930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132296719..132298590hg38UCSC Ensembl
Innerchr12:132873305..132875176hg19UCSC Ensembl
Innerchr12:131383378..131385249hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381872
hg191872
hg181872
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998915
Supporting Variants
SamplesHuRef
Known GenesGALNT9
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587234
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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