A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1737273



Internal ID12553705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14631933..14631933hg38UCSC Ensembl
chrX:14650055..14650055hg19UCSC Ensembl
chrX:14559976..14559976hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38264
hg19264
hg18264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4314219
SamplesHuRef
Known GenesGLRA2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1737273
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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