A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637374



Internal ID7024167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97288156..97357362hg38UCSC Ensembl
Innerchr15:97288156..97357362hg38UCSC Ensembl
Outerchr15:97287656..97357862hg38UCSC Ensembl
chr15:97831386..97900592hg19UCSC Ensembl
Innerchr15:97831386..97900592hg19UCSC Ensembl
Outerchr15:97830886..97901092hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3869207
hg1969207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15333418, essv15333417
SamplesNA18621, HG01124
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637374
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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