A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722221



Internal ID19020502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35224654..35511810hg38UCSC Ensembl
Innerchr16:34459025..34746181hg19UCSC Ensembl
Innerchr16:34316526..34603682hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38287157
hg19287157
hg18287157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056518
Supporting Variants
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722221
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