A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13412195



Internal ID2378132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17641247..17721211hg38UCSC Ensembl
chr9:17641245..17721209hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3879965
hg1979965
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619850
Supporting Variants
SamplesHG02107
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13412195
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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