A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037627



Internal ID18780158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14686785..14955789hg38UCSC Ensembl
Innerchr16:14780642..15049646hg19UCSC Ensembl
Innerchr16:14688143..14957147hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38269005
hg19269005
hg18269005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2740n100
Supporting Variantsnssv3557241
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037627
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