A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075719



Internal ID18971389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11758080..11758681hg38UCSC Ensembl
chrX:11776199..11776800hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772482
SamplesKWP1
Known GenesMSL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075719
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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