A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892647



Internal ID19183467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30816586..30887331hg38UCSC Ensembl
Outerchr15:30816586..30887331hg38UCSC Ensembl
Innerchr15:31108789..31179534hg19UCSC Ensembl
Outerchr15:31108789..31179534hg19UCSC Ensembl
Innerchr15:28896081..28966826hg18UCSC Ensembl
Outerchr15:28896081..28966826hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3870746
hg1970746
hg1870746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786619
Samples
Known GenesHERC2P10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892647
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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