A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1336683



Internal ID12499805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16183259..16183259hg38UCSC Ensembl
chrX:16201382..16201382hg19UCSC Ensembl
chrX:16111303..16111303hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3692084
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1336683
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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