A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636107



Internal ID7022903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34239088..34242962hg38UCSC Ensembl
Innerchr15:34239137..34242913hg38UCSC Ensembl
Outerchr15:34239039..34243011hg38UCSC Ensembl
chr15:34531289..34535163hg19UCSC Ensembl
Innerchr15:34531338..34535114hg19UCSC Ensembl
Outerchr15:34531240..34535212hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383875
hg193875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448e214
Supporting Variantsessv15210470
SamplesNA19700
Known GenesSLC12A6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636107
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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