A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637276



Internal ID7024070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93096724..93099592hg38UCSC Ensembl
Innerchr15:93096732..93099584hg38UCSC Ensembl
Outerchr15:93096716..93099600hg38UCSC Ensembl
chr15:93639953..93642821hg19UCSC Ensembl
Innerchr15:93639961..93642813hg19UCSC Ensembl
Outerchr15:93639945..93642829hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382869
hg192869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15321792
SamplesHG02568
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637276
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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