A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665895



Internal ID9585314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54834409..54834563hg38UCSC Ensembl
Outerchr19:54834372..54834613hg38UCSC Ensembl
Innerchr19:55345864..55346018hg19UCSC Ensembl
Outerchr19:55345827..55346068hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6223533
SamplesHG01108
Known GenesKIR2DS4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665895
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