A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076280



Internal ID18976860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149539266..149540655hg38UCSC Ensembl
chrX:148620799..148622200hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381390
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767846
SamplesKWP1
Known GenesLINC00893
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076280
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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