A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155270



Internal ID22085775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934328..19956040hg38UCSC Ensembl
Outerchr16:19933041..19958932hg38UCSC Ensembl
Innerchr16:19945650..19967362hg19UCSC Ensembl
Outerchr16:19944363..19970254hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3825892
hg1925892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109n97
Supporting Variantsnssv4011594, nssv4011597, nssv4011595, nssv4011600, nssv4011593, nssv4011599, nssv4011596, nssv4011592, nssv4011598
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155270
Frequency
Sample Size131
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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