A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593086



Internal ID18544681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14195839..14238761hg38UCSC Ensembl
Innerchr3:14237339..14280261hg19UCSC Ensembl
Innerchr3:14212343..14255265hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3842923
hg1942923
hg1842923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003121
Supporting Variants
Samples
Known GenesLSM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593086
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