A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637179



Internal ID7023973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88916427..88922476hg38UCSC Ensembl
Innerchr15:88916477..88922299hg38UCSC Ensembl
Outerchr15:88916290..88922613hg38UCSC Ensembl
chr15:89459658..89465707hg19UCSC Ensembl
Innerchr15:89459708..89465530hg19UCSC Ensembl
Outerchr15:89459521..89465844hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386050
hg196050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317017, essv15317016, essv15317005, essv15317019, essv15317025, essv15317008, essv15317001, essv15316996, essv15317018, essv15317014, essv15317015, essv15317011, essv15317021, essv15317007, essv15317023, essv15317000, essv15316997, essv15317022, essv15317010, essv15317004, essv15316998, essv15317002, essv15317020, essv15317006, essv15317012, essv15317024, essv15317003, essv15317009, essv15317013, essv15316999
SamplesNA20762, HG03484, HG02628, HG02337, HG02318, NA19020, NA18917, HG03464, HG03499, NA20291, HG02111, NA19130, HG02489, HG03045, HG03352, HG02571, NA19152, HG02450, HG02470, HG03294, HG03064, HG02667, HG02308, HG02814, HG02771, NA19818, HG02013, HG03538, HG02284, HG03196
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637179
Frequency
Sample Size2504
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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