A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709716



Internal ID15656986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10236394..10363930hg38UCSC Ensembl
Innerchr1:10296452..10423988hg19UCSC Ensembl
Innerchr1:10219039..10346575hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38127537
hg19127537
hg18127537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545381
Supporting Variants
Samples
Known GenesKIF1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709716
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer