A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6084551



Internal ID9074585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79491611..79641774hg38UCSC Ensembl
chr1:79957296..80107459hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38150164
hg19150164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659334
Supporting Variants
SamplesHG01048
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6084551
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