A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13380767



Internal ID6335683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3934397..3935415hg38UCSC Ensembl
Innerchr9:3934447..3935365hg38UCSC Ensembl
Outerchr9:3934338..3935474hg38UCSC Ensembl
chr9:3934397..3935415hg19UCSC Ensembl
Innerchr9:3934447..3935365hg19UCSC Ensembl
Outerchr9:3934338..3935474hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619322
Supporting Variants
SamplesNA19982
Known GenesGLIS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13380767
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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