A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732592



Internal ID19030873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13227749..13780941hg38UCSC Ensembl
Innerchr21:14600070..15153262hg19UCSC Ensembl
Innerchr21:13521941..14075133hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38553193
hg19553193
hg18553193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058318
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)nssv3732592
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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