A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076285



Internal ID18974297
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 StatusM
Merged Variants
Supporting Variantsnssv3763903
SamplesKWP1
Known GenesMECP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076285
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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