A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152108



Internal ID19200839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151330327..151334128hg38UCSC Ensembl
OuterchrX:150498799..150502600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383802
hg193802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996716
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152108
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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