A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956567



Internal ID18870178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:14402775..14402820hg38UCSC Ensembl
Outerchr3:14444277..14444330hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3846
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114355
Supporting Variants
SamplesKWS1
Known GenesSLC6A6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956567
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