A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636978



Internal ID6677085
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15301213
SamplesHG03159
Known GenesSH2D7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636978
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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