A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008366



Internal ID19097584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214640706..214682554hg38UCSC Ensembl
Innerchr2:215505430..215547278hg19UCSC Ensembl
Innerchr2:215213675..215255523hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3841849
hg1941849
hg1841849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4172n100
Supporting Variantsnssv3585687
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)nsv1008366
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