A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519522



Internal ID18817803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30437138..30517986hg38UCSC Ensembl
Innerchr12:30590071..30670919hg19UCSC Ensembl
Innerchr12:30481338..30562186hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3880849
hg1980849
hg1880849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050233
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)nssv3519522
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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