A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152776



Internal ID19195534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149334469..149339770hg38UCSC Ensembl
OuterchrX:148415999..148421300hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997814
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152776
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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