A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15231051



Internal ID4679243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42520475..42525596hg38UCSC Ensembl
Innerchr15:42520975..42525096hg38UCSC Ensembl
Outerchr15:42519475..42526596hg38UCSC Ensembl
chr15:42812673..42817794hg19UCSC Ensembl
Innerchr15:42813173..42817294hg19UCSC Ensembl
Outerchr15:42811673..42818794hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg385122
hg195122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636274
Supporting Variants
SamplesHG04202
Known GenesSNAP23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15231051
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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