A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064732



Internal ID18807263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51770004..52114137hg38UCSC Ensembl
Innerchr19:52273257..52617390hg19UCSC Ensembl
Innerchr19:56965069..57309202hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38344134
hg19344134
hg18344134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3626n100
Supporting Variantsnssv3575023, nssv3575024, nssv3724915, nssv3575022, nssv3575025
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)nsv1064732
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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