A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636850



Internal ID6676957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71119411..71128303hg38UCSC Ensembl
Innerchr15:71119461..71128253hg38UCSC Ensembl
Outerchr15:71119316..71128398hg38UCSC Ensembl
chr15:71411750..71420642hg19UCSC Ensembl
Innerchr15:71411800..71420592hg19UCSC Ensembl
Outerchr15:71411655..71420737hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388893
hg198893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15285112
SamplesHG02236
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636850
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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