A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995022



Internal ID19221478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107012519..107013119hg38UCSC Ensembl
Outerchr9:109774800..109775400hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144287
Supporting Variants
SamplesKWS1
Known GenesMIR548Q
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3995022
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