A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057361



Internal ID18799892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39633228..39820356hg38UCSC Ensembl
Innerchr19:40123868..40310996hg19UCSC Ensembl
Innerchr19:44815708..45002836hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38187129
hg19187129
hg18187129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3529n100
Supporting Variantsnssv3568207
Samples
Known GenesCLC, LEUTX, LGALS14, LGALS16, LGALS17A, LOC100129935
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057361
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer