A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1589319



Internal ID12405754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132070950..132070950hg38UCSC Ensembl
chr11:131940844..131940844hg19UCSC Ensembl
chr11:131446054..131446054hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4064338
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1589319
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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