A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011864



Internal ID19101082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12772..132364hg38UCSC Ensembl
Innerchr2:12772..132364hg19UCSC Ensembl
Innerchr2:2772..122364hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38119593
hg19119593
hg18119593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570493
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011864
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