A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770351



Internal ID19305831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10714759..10720960hg38UCSC Ensembl
chrX:10682799..10689000hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386202
hg196202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078667
Supporting Variants
SamplesKWP1
Known GenesMID1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770351
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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