A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636232



Internal ID7023028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40792864..40804007hg38UCSC Ensembl
Innerchr15:40792864..40804007hg38UCSC Ensembl
Outerchr15:40792364..40804507hg38UCSC Ensembl
chr15:41085062..41096205hg19UCSC Ensembl
Innerchr15:41085062..41096205hg19UCSC Ensembl
Outerchr15:41084562..41096705hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3811144
hg1911144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15228653
SamplesHG03782
Known GenesDNAJC17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636232
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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