A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153600



Internal ID19199873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2413558..2426659hg38UCSC Ensembl
OuterchrX:2331599..2344700hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3813102
hg1913102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002253
SamplesKWB1
Known GenesDHRSX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153600
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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