A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056676



Internal ID18799207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77105785..77820951hg38UCSC Ensembl
Innerchr16:77139682..77854848hg19UCSC Ensembl
Innerchr16:75697183..76412349hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38715167
hg19715167
hg18715167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559660
Samples
Known GenesADAMTS18, MON1B, NUDT7, SYCE1L, VAT1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056676
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