A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892741



Internal ID18836875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98979139..99618239hg38UCSC Ensembl
Outerchr15:98979139..99618239hg38UCSC Ensembl
Innerchr15:99522368..100158444hg19UCSC Ensembl
Outerchr15:99522368..100158444hg19UCSC Ensembl
Innerchr15:97339891..97975967hg18UCSC Ensembl
Outerchr15:97339891..97975967hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38639101
hg19636077
hg18636077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792584
Samples
Known GenesHSP90B2P, LRRC28, MEF2A, PGPEP1L, SYNM, TTC23
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892741
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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