A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010618



Internal ID19099835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51307168..51358971hg38UCSC Ensembl
Innerchr2:51534306..51586109hg19UCSC Ensembl
Innerchr2:51387810..51439613hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3851804
hg1951804
hg1851804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726025, nssv3726024
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)nsv1010618
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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