A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636043



Internal ID6676152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31004381..31007907hg38UCSC Ensembl
Innerchr15:31004401..31007887hg38UCSC Ensembl
Outerchr15:31004361..31007927hg38UCSC Ensembl
chr15:31296584..31300110hg19UCSC Ensembl
Innerchr15:31296604..31300090hg19UCSC Ensembl
Outerchr15:31296564..31300130hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383527
hg193527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15204085, essv15204084, essv15204083
SamplesNA19430, NA19374, NA19473
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636043
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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