A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636685



Internal ID7023479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61495475..61496653hg38UCSC Ensembl
Innerchr15:61495481..61496647hg38UCSC Ensembl
Outerchr15:61495469..61496659hg38UCSC Ensembl
chr15:61787674..61788852hg19UCSC Ensembl
Innerchr15:61787680..61788846hg19UCSC Ensembl
Outerchr15:61787668..61788858hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15264664, essv15264663
SamplesNA20806, NA18544
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636685
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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