A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637102



Internal ID7023896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84930948..84941537hg38UCSC Ensembl
Innerchr15:84931448..84941037hg38UCSC Ensembl
Outerchr15:84929948..84942537hg38UCSC Ensembl
chr15:85474179..85484768hg19UCSC Ensembl
Innerchr15:85474679..85484268hg19UCSC Ensembl
Outerchr15:85473179..85485768hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3810590
hg1910590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15313894
SamplesNA11930
Known GenesSLC28A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637102
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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