A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639446



Internal ID6679539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84835487..84941557hg38UCSC Ensembl
chr16:84869093..84975163hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38106071
hg19106071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15547084, essv15547085, essv15547086
SamplesHG01850, HG02058, HG02702
Known GenesCRISPLD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639446
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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