A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635941



Internal ID7022738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26006084..26012332hg38UCSC Ensembl
Innerchr15:26006084..26012332hg38UCSC Ensembl
Outerchr15:26005584..26012832hg38UCSC Ensembl
chr15:26251231..26257479hg19UCSC Ensembl
Innerchr15:26251231..26257479hg19UCSC Ensembl
Outerchr15:26250731..26257979hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386249
hg196249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15193295
SamplesHG02330
Known GenesLOC100128714
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635941
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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