A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768591



Internal ID18962723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15149230..15149295hg38UCSC Ensembl
Outerchr10:15191229..15191294hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078731
Supporting Variants
SamplesKWP1
Known GenesNMT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768591
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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