A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544902



Internal ID15985625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:925754..949435hg38UCSC Ensembl
Innerchr1:861134..884815hg19UCSC Ensembl
Innerchr1:850997..874678hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3823682
hg1923682
hg1823682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9n54
Supporting Variantsnssv707686
Samples
Known GenesNOC2L, SAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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