A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153093



Internal ID19203442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:14811077..14816178hg38UCSC Ensembl
OuterchrX:14829199..14834300hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998128
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153093
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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