A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637251



Internal ID7024045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91949662..91956536hg38UCSC Ensembl
Innerchr15:91949662..91956536hg38UCSC Ensembl
Outerchr15:91949478..91956746hg38UCSC Ensembl
chr15:92492892..92499766hg19UCSC Ensembl
Innerchr15:92492892..92499766hg19UCSC Ensembl
Outerchr15:92492708..92499976hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386875
hg196875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15319553, essv15319554
SamplesHG02727, HG03021
Known GenesSLCO3A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637251
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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