A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063173



Internal ID19152392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23639182..24338821hg38UCSC Ensembl
Innerchr19:23821984..24521623hg19UCSC Ensembl
Innerchr19:23613824..24313463hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38699640
hg19699640
hg18699640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3481n100
Supporting Variantsnssv3570644
Samples
Known GenesHAVCR1P1, RPSAP58, ZNF254, ZNF675, ZNF681, ZNF726
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063173
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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