A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061098



Internal ID18803629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13084083..13842387hg38UCSC Ensembl
Innerchr21:14456404..15214708hg19UCSC Ensembl
Innerchr21:13378275..14136579hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38758305
hg19758305
hg18758305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4379n100
Supporting Variantsnssv3732563
Samples
Known GenesANKRD30BP2, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061098
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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