A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055537



Internal ID18798068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57531862..57570612hg38UCSC Ensembl
Innerchr16:57565774..57604524hg19UCSC Ensembl
Innerchr16:56123275..56162025hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3838751
hg1938751
hg1838751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559352
Samples
Known GenesCCDC102A, GPR114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055537
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