A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997670



Internal ID19192494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:152764883..152782077hg38UCSC Ensembl
OuterchrX:151933399..151950600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3817195
hg1917202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148882
Supporting Variants
SamplesKWB1
Known GenesMAGEA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997670
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer