A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161377



Internal ID7906091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29710985..29923133hg38UCSC Ensembl
Innerchr15:30003189..30215336hg19UCSC Ensembl
Innerchr15:27790481..28002628hg18UCSC Ensembl
Innerchr15:27790481..28002628hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38212149
hg19212148
hg18212148
hg17212148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422463
Supporting Variants
SamplesND05461
Known GenesTJP1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161377
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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