A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6561377



Internal ID9740140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38548500..38550146hg38UCSC Ensembl
Outerchr8:38548463..38550196hg38UCSC Ensembl
Innerchr8:38406018..38407664hg19UCSC Ensembl
Outerchr8:38405981..38407714hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381734
hg191734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659625
Supporting Variants
SamplesNA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6561377
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