A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071707



Internal ID19319084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62064443..62066444hg38UCSC Ensembl
chr20:60639499..60641500hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762082
SamplesKWP1
Known GenesTAF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071707
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