A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999762



Internal ID19193256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2840358..2845859hg38UCSC Ensembl
OuterchrX:2758399..2763900hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152581
Supporting Variants
SamplesKWB1
Known GenesGYG2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999762
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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