A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998890



Internal ID19158427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42880892..42907860hg38UCSC Ensembl
Innerchr1:43346563..43373531hg19UCSC Ensembl
Innerchr1:43119150..43146118hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3826969
hg1926969
hg1826969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3479539
Samples
Known GenesLOC339539
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998890
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