A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621526



Internal ID7008394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113032681..113046509hg38UCSC Ensembl
chr9:115794961..115808789hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3813829
hg1913829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606579, essv13606578, essv13606577
SamplesNA18745, NA19331, HG03433
Known GenesZFP37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621526
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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