A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078674



Internal ID19319204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64254319..64258320hg38UCSC Ensembl
chrX:63474199..63478200hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767194
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078674
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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