A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990470



Internal ID18886207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96352699..96352754hg38UCSC Ensembl
Outerchr10:98112456..98112511hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137947
Supporting Variants
SamplesKWS2
Known GenesOPALIN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990470
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