A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599881



Internal ID18898162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21063624..21118406hg38UCSC Ensembl
Innerchr21:22435942..22490724hg19UCSC Ensembl
Innerchr21:21357813..21412595hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3854783
hg1954783
hg1854783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057445
Supporting Variants
Samples
Known GenesNCAM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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