A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055704



Internal ID19144923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1591066..1617288hg38UCSC Ensembl
Innerchr20:1571712..1597934hg19UCSC Ensembl
Innerchr20:1519712..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3826223
hg1926223
hg1826223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4238n100
Supporting Variantsnssv3599327, nssv3599328
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055704
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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