A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071696



Internal ID18974484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41277675..41278896hg38UCSC Ensembl
chr20:39906315..39907536hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768287
SamplesKWP1
Known GenesZHX3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071696
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