A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10026865



Internal ID5686024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98548918..98690993hg38UCSC Ensembl
chr1:99014474..99156549hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38142076
hg19142076
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3586905
Supporting Variants
SamplesNA19083
Known GenesSNX7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10026865
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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