A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637358



Internal ID7024151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96807088..96838105hg38UCSC Ensembl
Innerchr15:96807088..96838105hg38UCSC Ensembl
Outerchr15:96806588..96838605hg38UCSC Ensembl
chr15:97350318..97381335hg19UCSC Ensembl
Innerchr15:97350318..97381335hg19UCSC Ensembl
Outerchr15:97349818..97381835hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3831018
hg1931018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15330627, essv15330628
SamplesNA19746, NA19770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637358
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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