A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610248



Internal ID6650474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104874542..105072035hg38UCSC Ensembl
chr6:105322417..105519910hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38197494
hg19197494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12496762
SamplesNA11881
Known GenesLIN28B, LINC00577
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610248
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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