A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768898



Internal ID18962068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153687744..153689645hg38UCSC Ensembl
chrX:152953199..152955100hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075343
Supporting Variants
SamplesKWP1
Known GenesSLC6A8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768898
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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