A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636138



Internal ID7022934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35469006..35470118hg38UCSC Ensembl
Innerchr15:35469006..35470118hg38UCSC Ensembl
Outerchr15:35468676..35470423hg38UCSC Ensembl
chr15:35761207..35762319hg19UCSC Ensembl
Innerchr15:35761207..35762319hg19UCSC Ensembl
Outerchr15:35760877..35762624hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381113
hg191113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15214200
SamplesHG01846
Known GenesDPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636138
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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