A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15214200



Internal ID1987846
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636138
Supporting Variants
SamplesHG01846
Known GenesDPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15214200
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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