A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155327



Internal ID22085832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58936836..58940063hg38UCSC Ensembl
Outerchr16:58929716..58943781hg38UCSC Ensembl
Innerchr16:58970740..58973967hg19UCSC Ensembl
Outerchr16:58963620..58977685hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3814066
hg1914066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008810, nssv4008811, nssv4008812
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155327
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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