A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764575



Internal ID19315365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151329727..151334328hg38UCSC Ensembl
chrX:150498199..150502800hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384602
hg194602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078692
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764575
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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