A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3481823



Internal ID19069910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:30101311..30704226hg38UCSC Ensembl
Innerchr1:30574158..31177073hg19UCSC Ensembl
Innerchr1:30346745..30949660hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38602916
hg19602916
hg18602916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005851
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)nssv3481823
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