A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075337



Internal ID18977259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145816481..145822582hg38UCSC Ensembl
chrX:144897999..144904100hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768930
SamplesKWP1
Known GenesSLITRK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075337
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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