A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001341



Internal ID19090558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40787107..40981013hg38UCSC Ensembl
Innerchr2:41014247..41208153hg19UCSC Ensembl
Innerchr2:40867751..41061657hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38193907
hg19193907
hg18193907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581490
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)nsv1001341
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