A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637479



Internal ID7024271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100503579..100504272hg38UCSC Ensembl
Innerchr15:100503664..100504222hg38UCSC Ensembl
Outerchr15:100503529..100504322hg38UCSC Ensembl
chr15:101043784..101044477hg19UCSC Ensembl
Innerchr15:101043869..101044427hg19UCSC Ensembl
Outerchr15:101043734..101044527hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15352167, essv15352166, essv15352168
SamplesNA19023, NA19036, NA19445
Known GenesCERS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637479
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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