A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055206



Internal ID18797737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37267421..37621089hg38UCSC Ensembl
Innerchr20:35895824..36249491hg19UCSC Ensembl
Innerchr20:35329238..35682905hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38353669
hg19353668
hg18353668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584758
Samples
Known GenesBLCAP, LINC00489, MANBAL, NNAT, SRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055206
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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