A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16083570



Internal ID2164225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52390478..52468038hg38UCSC Ensembl
chr19:52893731..52971291hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3877561
hg1977561
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644693
Supporting Variants
SamplesHG01954
Known GenesZNF528, ZNF534, ZNF578
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16083570
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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