A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704836



Internal ID19003117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:187299634..187350227hg38UCSC Ensembl
Innerchr1:187268766..187319359hg19UCSC Ensembl
Innerchr1:185535389..185585982hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3850594
hg1950594
hg1850594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008401
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)nssv3704836
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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