A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544903



Internal ID15985626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:925754..952840hg38UCSC Ensembl
Innerchr1:861134..888220hg19UCSC Ensembl
Innerchr1:850997..878083hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3827087
hg1927087
hg1827087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9n54
Supporting Variantsnssv707687
Samples
Known GenesNOC2L, SAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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