A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6547624



Internal ID9525027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35253107..35263032hg38UCSC Ensembl
Outerchr19:35253070..35263082hg38UCSC Ensembl
Innerchr19:35744010..35753935hg19UCSC Ensembl
Outerchr19:35743973..35753985hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3810013
hg1910013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665499
Supporting Variants
SamplesHG00690
Known GenesLSR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6547624
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