A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978297



Internal ID19242638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61095142..61111894hg38UCSC Ensembl
Outerchr9:43846200..43862900hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816753
hg1916701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139960
Supporting Variants
SamplesKWS2
Known GenesCNTNAP3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978297
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