A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637126



Internal ID7023920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85813985..85821038hg38UCSC Ensembl
Innerchr15:85814024..85821000hg38UCSC Ensembl
Outerchr15:85813947..85821077hg38UCSC Ensembl
chr15:86357216..86364269hg19UCSC Ensembl
Innerchr15:86357255..86364231hg19UCSC Ensembl
Outerchr15:86357178..86364308hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387054
hg197054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15315829, essv15315830, essv15315832, essv15315833, essv15315824, essv15315827, essv15315828, essv15315825, essv15315826, essv15315831
SamplesNA20298, HG03385, HG02595, HG02461, HG02943, HG02666, HG03064, HG02580, HG03565, HG02808
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637126
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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