A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619823



Internal ID7006697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16882494..16885084hg38UCSC Ensembl
Innerchr9:16882494..16885084hg38UCSC Ensembl
Outerchr9:16882306..16885260hg38UCSC Ensembl
chr9:16882492..16885082hg19UCSC Ensembl
Innerchr9:16882492..16885082hg19UCSC Ensembl
Outerchr9:16882304..16885258hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg382591
hg192591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13411486, essv13411489, essv13411485, essv13411484, essv13411482, essv13411483, essv13411481, essv13411487, essv13411488
SamplesNA12717, HG01779, NA12044, HG03624, NA20753, HG00276, NA20773, HG00254, HG01205
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619823
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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