A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252158



Internal ID21308776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9163996..9167445hg38UCSC Ensembl
Outerchr19:9163124..9174084hg38UCSC Ensembl
Innerchr19:9274672..9278121hg19UCSC Ensembl
Outerchr19:9273800..9284760hg19UCSC Ensembl
Innerchr19:9135672..9139121hg18UCSC Ensembl
Outerchr19:9134800..9145760hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810961
hg1910961
hg1810961
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170267
Supporting Variants
SamplesNGO_45
Known GenesZNF317
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252158
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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