A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610774



Internal ID6997691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129629038..129636663hg38UCSC Ensembl
Innerchr6:129629038..129636663hg38UCSC Ensembl
Outerchr6:129628892..129636837hg38UCSC Ensembl
chr6:129950183..129957808hg19UCSC Ensembl
Innerchr6:129950183..129957808hg19UCSC Ensembl
Outerchr6:129950037..129957982hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg387626
hg197626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12546199
SamplesHG03786
Known GenesARHGAP18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610774
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