A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145268



Internal ID19280197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130378213..130378613hg38UCSC Ensembl
Outerchr9:133253600..133254000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4150n106
Supporting Variantsnssv3982355
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145268
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