A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271668



Internal ID5273484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64815095..64823057hg38UCSC Ensembl
Innerchr15:64815095..64823057hg38UCSC Ensembl
Outerchr15:64814595..64823557hg38UCSC Ensembl
chr15:65107294..65115256hg19UCSC Ensembl
Innerchr15:65107294..65115256hg19UCSC Ensembl
Outerchr15:65106794..65115756hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg387963
hg197963
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636745
Supporting Variants
SamplesNA19121
Known GenesPIF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271668
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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