A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1383760



Internal ID12546882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:124334518..124334704hg38UCSC Ensembl
chrX:123468368..123468554hg19UCSC Ensembl
chrX:123296049..123296235hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38187
hg19187
hg18187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4300305
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1383760
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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