A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060131



Internal ID18802662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35370865hg38UCSC Ensembl
Innerchr19:35849481..35861767hg19UCSC Ensembl
Innerchr19:40541321..40553607hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812287
hg1912287
hg1812287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3519n100
Supporting Variantsnssv3566675, nssv3724367, nssv3566671, nssv3566669, nssv3566678, nssv3566668, nssv3566674, nssv3566667, nssv3566673, nssv3724366, nssv3724365, nssv3566672, nssv3566677, nssv3566670, nssv3566676
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060131
Frequency
Sample Size29084
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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