A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119297



Internal ID19258651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63142128..63150228hg38UCSC Ensembl
Outerchr9:67047100..67055200hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg388101
hg198101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959734
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119297
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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