A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998262



Internal ID19192075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155981334..155987435hg38UCSC Ensembl
OuterchrX:155210999..155217100hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146898
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998262
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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