A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010042



Internal ID22071673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88080057..88081785hg38UCSC Ensembl
Outerchr16:88076816..88082524hg38UCSC Ensembl
Innerchr16:88113663..88115391hg19UCSC Ensembl
Outerchr16:88110422..88116130hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385709
hg195709
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155368
Supporting Variants
Samples
Known GenesBANP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010042
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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