A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116429



Internal ID21299695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19020759..19023283hg38UCSC Ensembl
Innerchr21:20393078..20395602hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382525
hg192525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv698n145
Supporting Variantsnssv14102103, nssv14101590, nssv14100900, nssv14100933, nssv14102020, nssv14101593, nssv14101951, nssv14102193, nssv14102092, nssv14100854, nssv14101618, nssv14100875
Samplessample119, sample83, sample303, sample211, sample7, sample140, sample293, sample395, sample117, sample46, sample27, sample150
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116429
Frequency
Sample Size467
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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