A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636578



Internal ID7023372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56225444..56240092hg38UCSC Ensembl
Innerchr15:56225944..56239592hg38UCSC Ensembl
Outerchr15:56224444..56241092hg38UCSC Ensembl
chr15:56517642..56532290hg19UCSC Ensembl
Innerchr15:56518142..56531790hg19UCSC Ensembl
Outerchr15:56516642..56533290hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3814649
hg1914649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15256421, essv15256422
SamplesNA19035, NA19428
Known GenesRFX7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636578
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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