A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110042



Internal ID19251989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:95864099..95864165hg38UCSC Ensembl
Outerchr9:98626381..98626447hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959276
SamplesKWS1
Known GenesLINC00476
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110042
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer