A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5435767



Internal ID9816392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34883655..34884589hg38UCSC Ensembl
chr1:35349256..35350190hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670062
Supporting Variants
SamplesNA19982
Known GenesDLGAP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5435767
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