A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969822



Internal ID18886424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:9773940..9774011hg38UCSC Ensembl
Outerchr16:9867797..9867868hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113753
Supporting Variants
SamplesKWS2
Known GenesGRIN2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969822
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