A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv721165



Internal ID16015121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108827521..108829252hg38UCSC Ensembl
Innerchr1:109370143..109371874hg19UCSC Ensembl
Innerchr1:109171666..109173397hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381732
hg191732
hg181732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547424
Supporting Variants
Samples
Known GenesAKNAD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv721165
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