A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3479153



Internal ID18721812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16902199..16921891hg38UCSC Ensembl
Innerchr1:17228694..17248386hg19UCSC Ensembl
Innerchr1:17101281..17120973hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3819693
hg1919693
hg1819693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997723
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)nssv3479153
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