A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110632



Internal ID19254739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151021627..151029628hg38UCSC Ensembl
OuterchrX:150190100..150198100hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg388002
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960287
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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