A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636663



Internal ID7023457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60365733..60378815hg38UCSC Ensembl
Innerchr15:60365733..60378815hg38UCSC Ensembl
Outerchr15:60365233..60379315hg38UCSC Ensembl
chr15:60657932..60671014hg19UCSC Ensembl
Innerchr15:60657932..60671014hg19UCSC Ensembl
Outerchr15:60657432..60671514hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813083
hg1913083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15262700
SamplesHG04156
Known GenesANXA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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