A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057290



Internal ID19146509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51770004..52111494hg38UCSC Ensembl
Innerchr19:52273257..52614747hg19UCSC Ensembl
Innerchr19:56965069..57306559hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38341491
hg19341491
hg18341491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3626n100
Supporting Variantsnssv3724914, nssv3724913, nssv3575021
Samples
Known GenesFPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, 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)nsv1057290
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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