A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153582



Internal ID19198732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:42004646..42011647hg38UCSC Ensembl
OuterchrX:41863899..41870900hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg387002
hg197002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002234
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153582
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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