A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763903



Internal ID18966894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154034248..154039549hg38UCSC Ensembl
chrX:153299699..153305000hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076285
Supporting Variants
SamplesKWP1
Known GenesMECP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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