A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600079



Internal ID18898360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:24360829..24414165hg38UCSC Ensembl
Innerchr21:25733142..25786479hg19UCSC Ensembl
Innerchr21:24655013..24708350hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3853337
hg1953338
hg1853338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065835
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600079
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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