A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077163



Internal ID18970289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91796717..91799218hg38UCSC Ensembl
chr9:94558999..94561500hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764289
SamplesKWP1
Known GenesROR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077163
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