A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077324



Internal ID19320306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125886130..125900231hg38UCSC Ensembl
chr10:127574699..127588800hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3814102
hg1914102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770239
SamplesKWP1
Known GenesFANK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077324
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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