A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620748



Internal ID6660929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76790905..76818145hg38UCSC Ensembl
chr9:79405821..79433061hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3827241
hg1927241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1484e214
Supporting Variantsessv13528562, essv13528564, essv13528561, essv13528563
SamplesNA19332, HG04094, HG02655, NA19922
Known GenesPRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620748
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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