A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056251



Internal ID18798782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29964373..29986456hg38UCSC Ensembl
Innerchr19:30455280..30477363hg19UCSC Ensembl
Innerchr19:35147120..35169203hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3822084
hg1922084
hg1822084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3511n100
Supporting Variantsnssv3566542
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)nsv1056251
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