A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6023090



Internal ID8863037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152283758..152324950hg38UCSC Ensembl
chr5:151663319..151704511hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3841193
hg1941193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669341
Supporting Variants
SamplesHG00319
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6023090
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