A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15320952



Internal ID1449829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92159180..92162317hg38UCSC Ensembl
Innerchr15:92159180..92162317hg38UCSC Ensembl
Outerchr15:92159055..92162510hg38UCSC Ensembl
chr15:92702410..92705547hg19UCSC Ensembl
Innerchr15:92702410..92705547hg19UCSC Ensembl
Outerchr15:92702285..92705740hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383138
hg193138
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637258
Supporting Variants
SamplesHG01342
Known GenesSLCO3A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15320952
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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