A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639448



Internal ID6679541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84893133..84934433hg38UCSC Ensembl
chr16:84926739..84968039hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3841301
hg1941301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15547090
SamplesHG02702
Known GenesCRISPLD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639448
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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