A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013566



Internal ID22075197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41553476..41555937hg38UCSC Ensembl
Outerchr19:41551655..41557305hg38UCSC Ensembl
Innerchr19:42059846..42062307hg19UCSC Ensembl
Outerchr19:42058025..42063675hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385651
hg195651
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155581
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013566
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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