A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978437



Internal ID19233064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:79927403..79932404hg38UCSC Ensembl
OuterchrX:79182900..79187900hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg385002
hg195001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115874
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978437
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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