A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596656



Internal ID6636926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77128452..77132285hg38UCSC Ensembl
chr3:77177603..77181436hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383834
hg193834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11048843, essv11048845, essv11048846, essv11048841, essv11048842, essv11048844
SamplesHG00344, HG02104, HG04206, HG03788, HG02087, HG02784
Known GenesROBO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596656
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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