A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589203



Internal ID6629492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235969032..235977454hg38UCSC Ensembl
Innerchr1:235969043..235977444hg38UCSC Ensembl
Outerchr1:235969022..235977465hg38UCSC Ensembl
chr1:236132332..236140754hg19UCSC Ensembl
Innerchr1:236132343..236140744hg19UCSC Ensembl
Outerchr1:236132322..236140765hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg388423
hg198423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10333146
SamplesHG02087
Known GenesNID1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589203
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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