A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545005



Internal ID16332414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1452075..1490320hg38UCSC Ensembl
Innerchr1:1387455..1425700hg19UCSC Ensembl
Innerchr1:1377318..1415563hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3838246
hg1938246
hg1838246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n54
Supporting Variantsnssv708590
Samples
Known GenesATAD3B, ATAD3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545005
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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