A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585280



Internal ID18883561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13197951..13775809hg38UCSC Ensembl
Innerchr21:14570272..15148130hg19UCSC Ensembl
Innerchr21:13492143..14070001hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38577859
hg19577859
hg18577859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056586
Supporting Variants
Samples
Known GenesLOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585280
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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