A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6584585



Internal ID9190628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53353576..53383224hg38UCSC Ensembl
chr19:53856829..53886477hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3829649
hg1929649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670793
Supporting Variants
SamplesHG01488
Known GenesZNF525, ZNF845
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6584585
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