A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13527184



Internal ID572122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75875596..75879730hg38UCSC Ensembl
Innerchr9:75875596..75879730hg38UCSC Ensembl
Outerchr9:75875218..75880077hg38UCSC Ensembl
chr9:78490512..78494646hg19UCSC Ensembl
Innerchr9:78490512..78494646hg19UCSC Ensembl
Outerchr9:78490134..78494993hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384135
hg194135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620731
Supporting Variants
SamplesHG00252
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13527184
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