A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15264663



Internal ID5081763
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636685
Supporting Variants
SamplesNA18544
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15264663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer