A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035263



Internal ID18777794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21557869..21828019hg38UCSC Ensembl
Innerchr16:21569190..21839340hg19UCSC Ensembl
Innerchr16:21476691..21746841hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38270151
hg19270151
hg18270151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2807n100
Supporting Variantsnssv3719306
Samples
Known GenesIGSF6, METTL9, OTOA, RRN3P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035263
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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