A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961332



Internal ID19222842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:59656096..59674933hg38UCSC Ensembl
Outerchr16:59690000..59708837hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3818838
hg1918838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110915
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961332
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer