A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3630965



Internal ID6671098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121979665..121992197hg38UCSC Ensembl
chr12:122417571..122430103hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3812533
hg1912533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14620028, essv14620026, essv14620029, essv14620027
SamplesNA20876, NA20851, NA21144, NA21107
Known GenesWDR66
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3630965
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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