A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636866



Internal ID6676973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71931082..71932790hg38UCSC Ensembl
Innerchr15:71931114..71932758hg38UCSC Ensembl
Outerchr15:71931050..71932822hg38UCSC Ensembl
chr15:72223423..72225131hg19UCSC Ensembl
Innerchr15:72223455..72225099hg19UCSC Ensembl
Outerchr15:72223391..72225163hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381709
hg191709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15287965
SamplesHG00446
Known GenesMYO9A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636866
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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