A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013442



Internal ID22075073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9163996..9167445hg38UCSC Ensembl
Outerchr19:9163124..9174084hg38UCSC Ensembl
Innerchr19:9274672..9278121hg19UCSC Ensembl
Outerchr19:9273800..9284760hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810961
hg1910961
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155550
Supporting Variants
Samples
Known GenesZNF317
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013442
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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