A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729299



Internal ID19027580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185983043..186083155hg38UCSC Ensembl
Innerchr2:186847770..186947882hg19UCSC Ensembl
Innerchr2:186556015..186656127hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38100113
hg19100113
hg18100113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007635
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)nssv3729299
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