A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12499082



Internal ID1150343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107041055..107042175hg38UCSC Ensembl
Innerchr6:107041110..107042121hg38UCSC Ensembl
Outerchr6:107041001..107042230hg38UCSC Ensembl
chr6:107362259..107363379hg19UCSC Ensembl
Innerchr6:107362314..107363325hg19UCSC Ensembl
Outerchr6:107362205..107363434hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610289
Supporting Variants
SamplesHG01028
Known GenesC6orf203
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12499082
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