A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13609581



Internal ID3239743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116584662..116587712hg38UCSC Ensembl
Innerchr9:116584688..116587686hg38UCSC Ensembl
Outerchr9:116584636..116587738hg38UCSC Ensembl
chr9:119346941..119349991hg19UCSC Ensembl
Innerchr9:119346967..119349965hg19UCSC Ensembl
Outerchr9:119346915..119350017hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383051
hg193051
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621588
Supporting Variants
SamplesHG02854
Known GenesASTN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13609581
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