A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544896



Internal ID15985619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:918574..934930hg38UCSC Ensembl
Innerchr1:853954..870310hg19UCSC Ensembl
Innerchr1:843817..860173hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3816357
hg1916357
hg1816357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n54
Supporting Variantsnssv707676
Samples
Known GenesLOC100130417, SAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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