A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585260



Internal ID18536855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13041804..13715620hg38UCSC Ensembl
Innerchr21:14414125..15087941hg19UCSC Ensembl
Innerchr21:13335996..14009812hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38673817
hg19673817
hg18673817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067181
Supporting Variants
Samples
Known GenesANKRD30BP2, LOC100288966, MIR3156-3, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585260
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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