A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637233



Internal ID7024027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90724356..90730686hg38UCSC Ensembl
Innerchr15:90724371..90730672hg38UCSC Ensembl
Outerchr15:90724342..90730701hg38UCSC Ensembl
chr15:91267587..91273917hg19UCSC Ensembl
Innerchr15:91267602..91273903hg19UCSC Ensembl
Outerchr15:91267573..91273932hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386331
hg196331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317410, essv15317409
SamplesNA19917, HG02076
Known GenesBLM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637233
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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