A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999478



Internal ID18840943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15149222..15149299hg38UCSC Ensembl
Outerchr10:15191221..15191298hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146274
Supporting Variants
SamplesKWB1
Known GenesNMT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999478
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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