A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151768



Internal ID19196641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:71999623..71999684hg38UCSC Ensembl
Outerchr14:72466340..72466401hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998953
SamplesKWB1
Known GenesRGS6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151768
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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