A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637353



Internal ID7024146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96539205..96546781hg38UCSC Ensembl
Innerchr15:96539216..96546771hg38UCSC Ensembl
Outerchr15:96539195..96546792hg38UCSC Ensembl
chr15:97082435..97090011hg19UCSC Ensembl
Innerchr15:97082446..97090001hg19UCSC Ensembl
Outerchr15:97082425..97090022hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg387577
hg197577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15329471, essv15329467, essv15329466, essv15329468, essv15329465, essv15329469, essv15329470
SamplesNA21111, HG04033, HG04183, HG03947, HG02780, NA20866, HG02657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637353
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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