A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1172590



Internal ID15529434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3680453..3755227hg38UCSC Ensembl
Innerchr1:3597017..3671791hg19UCSC Ensembl
Innerchr1:3586877..3661651hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3874775
hg1974775
hg1874775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545129
Supporting Variants
SamplesHGDP00787
Known GenesCCDC27, TP73, TP73-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1172590
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