A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518540



Internal ID15445833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39207334..39241143hg38UCSC Ensembl
Innerchr19:39697974..39731783hg19UCSC Ensembl
Innerchr19:44389814..44423623hg18UCSC Ensembl
Innerchr19:44389814..44423623hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3833810
hg1933810
hg1833810
hg1733810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695984
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518540
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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