A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057703



Internal ID19146922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35675245..35768349hg38UCSC Ensembl
Innerchr21:37047543..37140647hg19UCSC Ensembl
Innerchr21:35969413..36062517hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3893105
hg1993105
hg1893105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732703
Samples
Known GenesMIR802
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057703
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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