A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600102



Internal ID18898383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:27820466..27987620hg38UCSC Ensembl
Innerchr21:29192785..29359939hg19UCSC Ensembl
Innerchr21:28114656..28281810hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38167155
hg19167155
hg18167155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060376
Supporting Variants
Samples
Known GenesMIR5009
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600102
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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