A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619957



Internal ID7006830
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13419254
SamplesNA11932
Known GenesIFNA14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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