A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708411



Internal ID16002367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:934223..938178hg38UCSC Ensembl
Innerchr1:869603..873558hg19UCSC Ensembl
Innerchr1:859466..863421hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383956
hg193956
hg183956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544929
Supporting Variants
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708411
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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