A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709932



Internal ID16003888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11040115..11041925hg38UCSC Ensembl
Innerchr1:11100172..11101982hg19UCSC Ensembl
Innerchr1:11022759..11024569hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381811
hg191811
hg181811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545411
Supporting Variants
Samples
Known GenesMASP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709932
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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