A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637937



Internal ID7024724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11743320..11747541hg38UCSC Ensembl
chr16:11837176..11841397hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg384222
hg194222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377019, essv15377015, essv15377022, essv15377020, essv15377021, essv15377018, essv15377017, essv15377023, essv15377016
SamplesHG01485, HG03246, HG03040, NA18945, HG02839, HG03049, NA20289, HG03925, NA19711
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637937
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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