A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15206783



Internal ID5093648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32069590..32070813hg38UCSC Ensembl
Innerchr15:32069590..32070813hg38UCSC Ensembl
Outerchr15:32069332..32071018hg38UCSC Ensembl
chr15:32361793..32363016hg19UCSC Ensembl
Innerchr15:32361793..32363016hg19UCSC Ensembl
Outerchr15:32361535..32363221hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636071
Supporting Variants
SamplesNA18549
Known GenesCHRNA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15206783
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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