A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075416



Internal ID19325859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38271771..38280772hg38UCSC Ensembl
chr10:38560699..38569700hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg389002
hg199002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769031
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075416
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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