A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3736433



Internal ID19034714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130011844..130087197hg38UCSC Ensembl
Innerchr3:129730687..129806040hg19UCSC Ensembl
Innerchr3:131213377..131288730hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3875354
hg1975354
hg1875354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013916
Supporting Variants
Samples
Known GenesALG1L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3736433
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