A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547746



Internal ID15988469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143550435..143724450hg38UCSC Ensembl
Innerchr1:149045105..149219101hg19UCSC Ensembl
Innerchr1:147311729..147485725hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38174016
hg19173997
hg18173997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv539n54
Supporting Variantsnssv723297, nssv723296, nssv723298, nssv723299
Samples
Known GenesLOC101929780, NBPF23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547746
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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