A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057583



Internal ID18800114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54946627..55017462hg38UCSC Ensembl
Innerchr19:55457995..55528830hg19UCSC Ensembl
Innerchr19:60149807..60220642hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3870836
hg1970836
hg1870836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3679n100
Supporting Variantsnssv3570424, nssv3570425
Samples
Known GenesGP6, NLRP2, NLRP7, RNU6-35P, RNU6-64P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057583
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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