A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv722871



Internal ID16016827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:117336444..117339008hg38UCSC Ensembl
Innerchr1:117879066..117881630hg19UCSC Ensembl
Innerchr1:117680589..117683153hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg382565
hg192565
hg182565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547590
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv722871
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