A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610176



Internal ID6997095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101901530..102098696hg38UCSC Ensembl
chr6:102349405..102546571hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38197167
hg19197167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12485247
SamplesHG02003
Known GenesGRIK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610176
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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