A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059924



Internal ID18802455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51770004..52125358hg38UCSC Ensembl
Innerchr19:52273257..52628611hg19UCSC Ensembl
Innerchr19:56965069..57320423hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38355355
hg19355355
hg18355355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3626n100
Supporting Variantsnssv3575026, nssv3575027
Samples
Known GenesFPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF616, ZNF649, ZNF841
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059924
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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