A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6412922



Internal ID9769032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66661858..66745281hg38UCSC Ensembl
chr5:65957686..66041109hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3883424
hg1983424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676830
Supporting Variants
SamplesNA19726
Known GenesMAST4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6412922
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