A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966683



Internal ID18893124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:47533187..47628280hg38UCSC Ensembl
Outerchr10:47218900..47318300hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3895094
hg1999401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112582
Supporting Variants
SamplesKWS2
Known GenesBMS1P2, BMS1P6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966683
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