A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152581



Internal ID19202601
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 StatusM
Merged Variants
Supporting Variantsnssv3999762
SamplesKWB1
Known GenesGYG2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152581
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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