A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13633345



Internal ID1021541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131781647..131788081hg38UCSC Ensembl
Innerchr9:131781647..131788081hg38UCSC Ensembl
Outerchr9:131781401..131788346hg38UCSC Ensembl
chr9:134657034..134663468hg19UCSC Ensembl
Innerchr9:134657034..134663468hg19UCSC Ensembl
Outerchr9:134656788..134663733hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg386435
hg196435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621899
Supporting Variants
SamplesHG00640
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13633345
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