A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148075



Internal ID19201587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:96627545..96627640hg38UCSC Ensembl
Outerchr14:97093882..97093977hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001590
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148075
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer