A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636181



Internal ID7022977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37850054..37851312hg38UCSC Ensembl
Innerchr15:37850054..37851312hg38UCSC Ensembl
Outerchr15:37849702..37851542hg38UCSC Ensembl
chr15:38142255..38143513hg19UCSC Ensembl
Innerchr15:38142255..38143513hg19UCSC Ensembl
Outerchr15:38141903..38143743hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15220246, essv15220248, essv15220247, essv15220250, essv15220249
SamplesHG00189, HG00325, HG00365, HG00360, HG00368
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636181
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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