A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055624



Internal ID18798155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45719911..45752208hg38UCSC Ensembl
Innerchr20:44348550..44380847hg19UCSC Ensembl
Innerchr20:43781964..43814254hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3832298
hg1932298
hg1832291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3731337, nssv3584892, nssv3731336
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055624
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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