A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056576



Internal ID19145795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24304880..24413936hg38UCSC Ensembl
Innerchr19:24487682..24596738hg19UCSC Ensembl
Innerchr19:24279522..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38109057
hg19109057
hg18109057
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3491n100
Supporting Variantsnssv3570750, nssv3570744, nssv3570753, nssv3570746, nssv3570754, nssv3570751, nssv3570749, nssv3570747, nssv3570755, nssv3570756, nssv3570748, nssv3570752, nssv3570745
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056576
Frequency
Sample Size11257
Observed Gain9
Observed Loss4
Observed Complex0
Frequencyn/a


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