A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146881



Internal ID18850021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30526444..30526745hg38UCSC Ensembl
Outerchr19:31017351..31017652hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998240
SamplesKWB1
Known GenesZNF536
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146881
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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