A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065222



Internal ID18807753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50581448..50633587hg38UCSC Ensembl
Innerchr19:51084705..51136844hg19UCSC Ensembl
Innerchr19:55776517..55828656hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3852140
hg1952140
hg1852140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574994
Samples
Known GenesSNAR-F, SYT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065222
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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