A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639581



Internal ID6679672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89468407..89474358hg38UCSC Ensembl
Innerchr16:89468407..89474358hg38UCSC Ensembl
Outerchr16:89468247..89474567hg38UCSC Ensembl
chr16:89534815..89540766hg19UCSC Ensembl
Innerchr16:89534815..89540766hg19UCSC Ensembl
Outerchr16:89534655..89540975hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg385952
hg195952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569819
SamplesHG02154
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639581
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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