A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635823



Internal ID6675934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22867128..22867847hg38UCSC Ensembl
Innerchr15:22867178..22867797hg38UCSC Ensembl
Outerchr15:22867078..22867897hg38UCSC Ensembl
chr15:23005221..23005940hg19UCSC Ensembl
Innerchr15:23005271..23005890hg19UCSC Ensembl
Outerchr15:23005171..23005990hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15176458
SamplesHG01944
Known GenesNIPA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635823
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