A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563565



Internal ID6688607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:13879754..13885722hg38UCSC Ensembl
OuterchrX:13897873..13903841hg19UCSC Ensembl
OuterchrX:13807794..13813762hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385969
hg195969
hg185969
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991320
Supporting Variants
SamplesHuRef
Known GenesGPM6B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563565
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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