A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768892



Internal ID19306255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41837009..41885273hg38UCSC Ensembl
chr10:42354899..42403200hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3848265
hg1948302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075417
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768892
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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