A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15547086



Internal ID5548903
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639446
Supporting Variants
SamplesHG02702
Known GenesCRISPLD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15547086
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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