A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057530



Internal ID18800061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29978176..30039611hg38UCSC Ensembl
Innerchr19:30469083..30530518hg19UCSC Ensembl
Innerchr19:35160923..35222358hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3861436
hg1961436
hg1861436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3513n100
Supporting Variantsnssv3566565
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057530
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