A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10665107



Internal ID666923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128316086..128367910hg38UCSC Ensembl
chr2:129073660..129125484hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3851825
hg1951825
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3592386
Supporting Variants
SamplesNA19440
Known GenesHS6ST1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10665107
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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