A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451499



Internal ID15298444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155075297..155075297hg38UCSC Ensembl
InnerchrX:155075296..155075298hg38UCSC Ensembl
OuterchrX:155075237..155075347hg38UCSC Ensembl
chrX:154303572..154303572hg19UCSC Ensembl
InnerchrX:154303571..154303573hg19UCSC Ensembl
OuterchrX:154303512..154303622hg19UCSC Ensembl
chrX:153956766..153956766hg18UCSC Ensembl
InnerchrX:153956767..153956765hg18UCSC Ensembl
OuterchrX:153956706..153956816hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8846716
SamplesNA19240
Known GenesBRCC3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451499
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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