A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585245



Internal ID16372654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1583892..1611843hg38UCSC Ensembl
Innerchr20:1564538..1592489hg19UCSC Ensembl
Innerchr20:1512538..1540489hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3827952
hg1927952
hg1827952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7434n54
Supporting Variantsnssv936148, nssv936157, nssv936152, nssv936140, nssv936145, nssv936155, nssv936144, nssv936164, nssv936143, nssv936161, nssv936141, nssv936159, nssv936162, nssv936142, nssv936147, nssv936150, nssv936146, nssv936158, nssv936149, nssv936151, nssv936166, nssv936167, nssv936163, nssv936160, nssv936153, nssv936154, nssv936156, nssv936165
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585245
Frequency
Sample Size17421
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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