A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636306



Internal ID7023102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44305280..44314329hg38UCSC Ensembl
Innerchr15:44305430..44314179hg38UCSC Ensembl
Outerchr15:44305130..44314479hg38UCSC Ensembl
chr15:44597478..44606527hg19UCSC Ensembl
Innerchr15:44597628..44606377hg19UCSC Ensembl
Outerchr15:44597328..44606677hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg389050
hg199050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233230
SamplesHG01890
Known GenesCASC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636306
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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