A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13456372



Internal ID2663149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33484761..33510090hg38UCSC Ensembl
chr9:33484759..33510088hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3825330
hg1925330
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620326
Supporting Variants
SamplesHG02356
Known GenesSUGT1P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13456372
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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