A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545672



Internal ID15986395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16856620..16973488hg38UCSC Ensembl
Innerchr1:17183115..17299983hg19UCSC Ensembl
Innerchr1:17055702..17172570hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38116869
hg19116869
hg18116869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710897
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545672
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