A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076718



Internal ID19321920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101471911..101479112hg38UCSC Ensembl
chrX:100726899..100734100hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg387202
hg197202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764939
SamplesKWP1
Known GenesARMCX4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076718
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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