A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15210470



Internal ID6154847
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636107
Supporting Variants
SamplesNA19700
Known GenesSLC12A6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15210470
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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