A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011969



Internal ID18754505
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3467774, nssv3465593
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)nsv1011969
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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