A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762281



Internal ID19310519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10999379..11002080hg38UCSC Ensembl
chrX:11017499..11020200hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078668
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762281
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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