A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465593



Internal ID18714615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15826990..15875045hg38UCSC Ensembl
Innerchr1:16153485..16201540hg19UCSC Ensembl
Innerchr1:16026072..16074127hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3848056
hg1948056
hg1848056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011969
Supporting Variants
Samples
Known GenesFLJ37453, SPEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3465593
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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