A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055627



Internal ID18798158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54835663..54867232hg38UCSC Ensembl
Innerchr19:55347118..55378687hg19UCSC Ensembl
Innerchr19:60038930..60070499hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3831570
hg1931570
hg1831570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3678n100
Supporting Variantsnssv3570419
Samples
Known GenesKIR2DS4, KIR3DL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055627
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