A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636110



Internal ID7022906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34296496..34300745hg38UCSC Ensembl
Innerchr15:34296546..34300695hg38UCSC Ensembl
Outerchr15:34296446..34300795hg38UCSC Ensembl
chr15:34588697..34592946hg19UCSC Ensembl
Innerchr15:34588747..34592896hg19UCSC Ensembl
Outerchr15:34588647..34592996hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384250
hg194250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15210530, essv15210534, essv15210529, essv15210533, essv15210531, essv15210532
SamplesHG03105, HG02420, NA19663, HG02555, HG03354, HG02546
Known GenesSLC12A6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636110
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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