A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002662



Internal ID18745194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175655807..176170259hg38UCSC Ensembl
Innerchr3:175373595..175888047hg19UCSC Ensembl
Innerchr3:176856289..177370741hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38514453
hg19514453
hg18514453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613624
Samples
Known GenesNAALADL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002662
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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