A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6369820



Internal ID9700625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17196073..17200398hg38UCSC Ensembl
Outerchr6:17196036..17200448hg38UCSC Ensembl
Innerchr6:17196304..17200629hg19UCSC Ensembl
Outerchr6:17196267..17200679hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384413
hg194413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659689
Supporting Variants
SamplesNA19451
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6369820
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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