A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13459062



Internal ID6041754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34935418..34938753hg38UCSC Ensembl
Innerchr9:34935477..34938695hg38UCSC Ensembl
Outerchr9:34935360..34938812hg38UCSC Ensembl
chr9:34935415..34938750hg19UCSC Ensembl
Innerchr9:34935474..34938692hg19UCSC Ensembl
Outerchr9:34935357..34938809hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383336
hg193336
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620365
Supporting Variants
SamplesNA19443
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13459062
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