A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075415



Internal ID19319433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30109770..30110671hg38UCSC Ensembl
chr10:30398699..30399600hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771770
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075415
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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