A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620768



Internal ID6660949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77186688..77228922hg38UCSC Ensembl
Innerchr9:77186701..77228910hg38UCSC Ensembl
Outerchr9:77186676..77228935hg38UCSC Ensembl
chr9:79801604..79843838hg19UCSC Ensembl
Innerchr9:79801617..79843826hg19UCSC Ensembl
Outerchr9:79801592..79843851hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3842235
hg1942235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13531840
SamplesHG03888
Known GenesVPS13A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620768
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