A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150694



Internal ID19197454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:145299..239200hg38UCSC Ensembl
Outerchr19:145299..239200hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3893902
hg1993902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996165
SamplesKWB1
Known GenesLINC01002
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150694
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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