A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636911



Internal ID6677018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74855500..74868960hg38UCSC Ensembl
Innerchr15:74855650..74868810hg38UCSC Ensembl
Outerchr15:74855350..74869110hg38UCSC Ensembl
chr15:75147841..75161301hg19UCSC Ensembl
Innerchr15:75147991..75161151hg19UCSC Ensembl
Outerchr15:75147691..75161451hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3813461
hg1913461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292833
SamplesHG01679
Known GenesSCAMP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636911
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