A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151378



Internal ID15508300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57298468..57365865hg38UCSC Ensembl
Innerchr20:55873524..55940921hg19UCSC Ensembl
Innerchr20:55306931..55374328hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3867398
hg1967398
hg1867398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586311
Supporting Variants
Samples1780862408_A
Known GenesMIR4325, MIR5095, MTRNR2L3, RAE1, SPO11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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