A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608236



Internal ID6995166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18326788..18331521hg38UCSC Ensembl
Innerchr6:18326788..18331521hg38UCSC Ensembl
Outerchr6:18326623..18331735hg38UCSC Ensembl
chr6:18327019..18331752hg19UCSC Ensembl
Innerchr6:18327019..18331752hg19UCSC Ensembl
Outerchr6:18326854..18331966hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12205174, essv12205175
SamplesHG01849, NA18546
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608236
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer