A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148760



Internal ID19197799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40645932..40646265hg38UCSC Ensembl
OuterchrX:40505184..40505517hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997544
SamplesKWB1
Known GenesCXorf38
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148760
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer