A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153854



Internal ID19200608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:63208820..63290023hg38UCSC Ensembl
OuterchrX:62428699..62509900hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3881204
hg1981202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002508
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153854
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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