A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057641



Internal ID19146860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1579885..1613191hg38UCSC Ensembl
Innerchr20:1560531..1593837hg19UCSC Ensembl
Innerchr20:1508531..1541837hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833307
hg1933307
hg1833307
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3591551, nssv3728382, nssv3591547, nssv3591548, nssv3591544, nssv3591550, nssv3728384, nssv3591545, nssv3591546, nssv3591552, nssv3728383, nssv3591553, nssv3591549
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)nsv1057641
Frequency
Sample Size11257
Observed Gain12
Observed Loss1
Observed Complex0
Frequencyn/a


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