A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637026



Internal ID6677133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80781097..80785564hg38UCSC Ensembl
Innerchr15:80781097..80785564hg38UCSC Ensembl
Outerchr15:80780819..80785726hg38UCSC Ensembl
chr15:81073438..81077905hg19UCSC Ensembl
Innerchr15:81073438..81077905hg19UCSC Ensembl
Outerchr15:81073160..81078067hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384468
hg194468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15305570
SamplesHG02879
Known GenesKIAA1199
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637026
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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