A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063558



Internal ID19152777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54270335hg38UCSC Ensembl
Innerchr19:54730202..54774189hg19UCSC Ensembl
Innerchr19:59422014..59466001hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3844007
hg1943988
hg1843988
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3658n100
Supporting Variantsnssv3726559, nssv3573393, nssv3573394, nssv3573390, nssv3573391, nssv3726560, nssv3573392
Samples
Known GenesLILRA6, LILRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063558
Frequency
Sample Size11257
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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