A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6178473



Internal ID9153140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32584325..32591396hg38UCSC Ensembl
chr1:33049926..33056997hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg387072
hg197072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671633
Supporting Variants
SamplesHG01342
Known GenesZBTB8A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6178473
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