A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608903



Internal ID6995827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47730386..47734637hg38UCSC Ensembl
Innerchr6:47730386..47734637hg38UCSC Ensembl
Outerchr6:47730211..47734791hg38UCSC Ensembl
chr6:47698122..47702373hg19UCSC Ensembl
Innerchr6:47698122..47702373hg19UCSC Ensembl
Outerchr6:47697947..47702527hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg384252
hg194252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12342486
SamplesHG04096
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608903
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