A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997813



Internal ID19188941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3966858..3968259hg38UCSC Ensembl
OuterchrX:3884899..3886300hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152778
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997813
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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