A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066434



Internal ID18808965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54786419..54835710hg38UCSC Ensembl
Innerchr19:55297871..55347165hg19UCSC Ensembl
Innerchr19:59989683..60038977hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3849292
hg1949295
hg1849295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3673n100
Supporting Variantsnssv3570242, nssv3570241
Samples
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066434
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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