A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585563



Internal ID18883844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:205104414..205199830hg38UCSC Ensembl
Innerchr2:205969138..206064554hg19UCSC Ensembl
Innerchr2:205677383..205772799hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3895417
hg1995417
hg1895417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000779
Supporting Variants
Samples
Known GenesPARD3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585563
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