A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13618756



Internal ID6032484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124843049..124849474hg38UCSC Ensembl
Innerchr9:124843549..124848974hg38UCSC Ensembl
Outerchr9:124842049..124850474hg38UCSC Ensembl
chr9:127605328..127611753hg19UCSC Ensembl
Innerchr9:127605828..127611253hg19UCSC Ensembl
Outerchr9:127604328..127612753hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386426
hg196426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621726
Supporting Variants
SamplesNA19438
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13618756
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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