A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572873



Internal ID16360282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62680059..62758607hg38UCSC Ensembl
Innerchr16:62713963..62792511hg19UCSC Ensembl
Innerchr16:61271464..61350012hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3878549
hg1978549
hg1878549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5173n54
Supporting Variantsnssv1149176
SamplesHGDP00155
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572873
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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