A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974471



Internal ID18894338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101090833..101090923hg38UCSC Ensembl
Outerchr4:102011990..102012080hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114560
Supporting Variants
SamplesKWS2
Known GenesPPP3CA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974471
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