A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637537



Internal ID6677641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65681..100253hg38UCSC Ensembl
chr16:115679..150251hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3834573
hg1934573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354662, essv15354664, essv15354663, essv15354661
SamplesHG03960, HG00524, HG01486, HG04054
Known GenesMPG, NPRL3, RHBDF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637537
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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