A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628647



Internal ID3630463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129701704..129885823hg38UCSC Ensembl
chr9:132463983..132648102hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38184120
hg19184120
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621839
Supporting Variants
SamplesHG03844
Known GenesC9orf78, MIR6855, PRRX2, PTGES, TOR1A, TOR1B, USP20
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628647
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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