A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732565



Internal ID19030846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13197951..13699835hg38UCSC Ensembl
Innerchr21:14570272..15072156hg19UCSC Ensembl
Innerchr21:13492143..13994027hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38501885
hg19501885
hg18501885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063022
Supporting Variants
Samples
Known GenesLOC100288966, 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)nssv3732565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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