A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545737



Internal ID16333146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21632043..21662129hg38UCSC Ensembl
Innerchr1:21958536..21988622hg19UCSC Ensembl
Innerchr1:21831123..21861209hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3830087
hg1930087
hg1830087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173794
Samples1780854065_A
Known GenesRAP1GAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545737
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