A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5449695



Internal ID9232790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39824798..39839004hg38UCSC Ensembl
Outerchr9:39824427..39839374hg38UCSC Ensembl
Innerchr9:41969816..41984022hg19UCSC Ensembl
Outerchr9:41969445..41984392hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814948
hg1914948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2662901
Supporting Variants
SamplesNA11920
Known GenesKGFLP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5449695
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