A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636479



Internal ID7023273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52012738..52015881hg38UCSC Ensembl
Innerchr15:52012738..52015881hg38UCSC Ensembl
Outerchr15:52012630..52016049hg38UCSC Ensembl
chr15:52304935..52308078hg19UCSC Ensembl
Innerchr15:52304935..52308078hg19UCSC Ensembl
Outerchr15:52304827..52308246hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383144
hg193144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15248859, essv15248858
SamplesNA19043, HG02941
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636479
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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