A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070001



Internal ID19321408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2385642..2385705hg38UCSC Ensembl
chr11:2406872..2406935hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763108
SamplesKWP1
Known GenesCD81
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070001
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