A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636167



Internal ID6676276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36977715..36987754hg38UCSC Ensembl
Innerchr15:36977715..36987754hg38UCSC Ensembl
Outerchr15:36977712..36987882hg38UCSC Ensembl
chr15:37269916..37279955hg19UCSC Ensembl
Innerchr15:37269916..37279955hg19UCSC Ensembl
Outerchr15:37269913..37280083hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3810040
hg1910040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15217026
SamplesNA18963
Known GenesMEIS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636167
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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