A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892715



Internal ID19183535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77010628..77035230hg38UCSC Ensembl
Outerchr15:77010628..77035230hg38UCSC Ensembl
Innerchr15:77302969..77327571hg19UCSC Ensembl
Outerchr15:77302969..77327571hg19UCSC Ensembl
Innerchr15:75090024..75114626hg18UCSC Ensembl
Outerchr15:75090024..75114626hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3824603
hg1924603
hg1824603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785254
Samples
Known GenesPSTPIP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892715
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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