A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13419254



Internal ID4799248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21238436..21267281hg38UCSC Ensembl
chr9:21238435..21267280hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828846
hg1928846
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619957
Supporting Variants
SamplesNA11932
Known GenesIFNA14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13419254
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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