A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6023799



Internal ID9001202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155689968..155694673hg38UCSC Ensembl
chr1:155659759..155664464hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg384706
hg194706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662699
Supporting Variants
SamplesNA18912
Known GenesDAP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6023799
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