A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993178



Internal ID19227427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47629901..47635401hg38UCSC Ensembl
OuterchrX:47489300..47494800hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141672
Supporting Variants
SamplesKWS2
Known GenesCFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993178
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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