A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638360



Internal ID7025146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29309350..29341486hg38UCSC Ensembl
chr16:29320671..29352807hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3832137
hg1932137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441404
SamplesHG02380
Known GenesSNX29P2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638360
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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