A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961232



Internal ID19215755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:142501493..142501565hg38UCSC Ensembl
Outerchr8:143582854..143582926hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110823
Supporting Variants
SamplesKWS1
Known GenesBAI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961232
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