A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621735



Internal ID7008602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125163680..125168991hg38UCSC Ensembl
Innerchr9:125163680..125168991hg38UCSC Ensembl
Outerchr9:125163393..125169267hg38UCSC Ensembl
chr9:127925959..127931270hg19UCSC Ensembl
Innerchr9:127925959..127931270hg19UCSC Ensembl
Outerchr9:127925672..127931546hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385312
hg195312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618911
SamplesHG00476
Known GenesPPP6C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621735
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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