A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961653



Internal ID19211123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:170900..178400hg38UCSC Ensembl
Outerchr9:170900..178400hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg387501
hg197501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128982
Supporting Variants
SamplesKWS1
Known GenesCBWD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961653
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