A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15301213



Internal ID5303029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78090507..78093028hg38UCSC Ensembl
Innerchr15:78090529..78093007hg38UCSC Ensembl
Outerchr15:78090486..78093050hg38UCSC Ensembl
chr15:78382849..78385370hg19UCSC Ensembl
Innerchr15:78382871..78385349hg19UCSC Ensembl
Outerchr15:78382828..78385392hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382522
hg192522
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636978
Supporting Variants
SamplesHG03159
Known GenesSH2D7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15301213
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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