A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151326



Internal ID19199331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:16230476..16236277hg38UCSC Ensembl
OuterchrX:16248599..16254400hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003889
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151326
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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