A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1057853



Internal ID11874292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134449370..134449370hg38UCSC Ensembl
chr6:134770508..134770508hg19UCSC Ensembl
chr6:134812201..134812201hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3936342
SamplesHuRef
Known GenesLINC01010
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1057853
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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