A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3468988



Internal ID18716449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12797714..12822696hg38UCSC Ensembl
Innerchr1:12857863..12882559hg19UCSC Ensembl
Innerchr1:12780450..12805146hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3824983
hg1924697
hg1824697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010023
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3468988
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