A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976667



Internal ID19237119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:25247771..25253771hg38UCSC Ensembl
Outerchr10:25536700..25542700hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124613
Supporting Variants
SamplesKWS2
Known GenesGPR158
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976667
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