A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056787



Internal ID18799318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14035183..14157970hg38UCSC Ensembl
Innerchr21:15407504..15530291hg19UCSC Ensembl
Innerchr21:14329375..14452162hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38122788
hg19122788
hg18122788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586454
Samples
Known GenesLIPI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056787
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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