A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636488



Internal ID7023282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52559024..52560705hg38UCSC Ensembl
Innerchr15:52559036..52560693hg38UCSC Ensembl
Outerchr15:52559012..52560717hg38UCSC Ensembl
chr15:52851221..52852902hg19UCSC Ensembl
Innerchr15:52851233..52852890hg19UCSC Ensembl
Outerchr15:52851209..52852914hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381682
hg191682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15249328
SamplesHG02696
Known GenesARPP19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636488
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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