A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563620



Internal ID7036380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150382393..150383294hg38UCSC Ensembl
OuterchrX:149550661..149551562hg19UCSC Ensembl
OuterchrX:149301319..149302220hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38902
hg19902
hg18902
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003742
Supporting Variants
SamplesHuRef
Known GenesMAMLD1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563620
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer