A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9841977



Internal ID6467270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3611161..3686920hg38UCSC Ensembl
chr1:3527725..3603484hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3875760
hg1975760
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585045
Supporting Variants
SamplesNA20872
Known GenesMEGF6, TP73, TPRG1L, WRAP73
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9841977
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer