A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708370



Internal ID15655640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:934170..938178hg38UCSC Ensembl
Innerchr1:869550..873558hg19UCSC Ensembl
Innerchr1:859413..863421hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg384009
hg194009
hg184009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544924
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)nssv708370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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