A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705726



Internal ID15442378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:185958561..185962797hg38UCSC Ensembl
Innerchr3:185676350..185680586hg19UCSC Ensembl
Innerchr3:187159044..187163280hg18UCSC Ensembl
Innerchr3:187159052..187163288hg17UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg384237
hg194237
hg184237
hg174237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529015
Supporting Variants
Samples
Known GenesLOC344887
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705726
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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