A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572835



Internal ID16360244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60722963..60762537hg38UCSC Ensembl
Innerchr16:60756867..60796441hg19UCSC Ensembl
Innerchr16:59314368..59353942hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3839575
hg1939575
hg1839575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149172
Samples1782681096_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572835
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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