A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13472271



Internal ID5859877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39826173..39840699hg38UCSC Ensembl
chr9:41971191..41985717hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814527
hg1914527
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620460
Supporting Variants
SamplesNA19236
Known GenesKGFLP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13472271
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