A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639447



Internal ID6679540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84838490..84875134hg38UCSC Ensembl
chr16:84872096..84908740hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3836645
hg1936645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15547087, essv15547088, essv15547089
SamplesHG01850, HG02058, HG02702
Known GenesCRISPLD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639447
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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