A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250032



Internal ID21303795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88080057..88081785hg38UCSC Ensembl
Outerchr16:88076816..88082524hg38UCSC Ensembl
Innerchr16:88113663..88115391hg19UCSC Ensembl
Outerchr16:88110422..88116130hg19UCSC Ensembl
Innerchr16:86671164..86672892hg18UCSC Ensembl
Outerchr16:86667923..86673631hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385709
hg195709
hg185709
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169992
Supporting Variants
SamplesMLY_9
Known GenesBANP
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250032
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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