A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074856



Internal ID18974289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93580593..93585094hg38UCSC Ensembl
chr5:92916299..92920800hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg384502
hg194502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765924
SamplesKWP1
Known GenesNR2F1, NR2F1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074856
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