A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076710



Internal ID19321930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56693966..56701567hg38UCSC Ensembl
chrX:56720399..56728000hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg387602
hg197602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763302
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076710
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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