A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv964220



Internal ID16258176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66500277..66501224hg38UCSC Ensembl
Innerchr3:66550701..66551648hg19UCSC Ensembl
Innerchr3:66633391..66634338hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38948
hg19948
hg18948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590555
Supporting Variants
Samples
Known GenesLRIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv964220
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