A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608033



Internal ID6994964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8592255..8650592hg38UCSC Ensembl
chr6:8592488..8650825hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3858338
hg1958338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12184537
SamplesHG01528
Known GenesLOC100506207
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608033
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