A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636842



Internal ID7023636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70631672..70638221hg38UCSC Ensembl
Innerchr15:70631698..70638196hg38UCSC Ensembl
Outerchr15:70631647..70638247hg38UCSC Ensembl
chr15:70924011..70930560hg19UCSC Ensembl
Innerchr15:70924037..70930535hg19UCSC Ensembl
Outerchr15:70923986..70930586hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386550
hg196550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv454e214
Supporting Variantsessv15284109
SamplesHG03478
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636842
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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