A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5928472



Internal ID8905875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29614477..29615373hg38UCSC Ensembl
chr21:30986797..30987693hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676813
Supporting Variants
SamplesNA19102
Known GenesGRIK1, GRIK1-AS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5928472
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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