A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568688



Internal ID18520283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42751053..42839327hg38UCSC Ensembl
Innerchr19:43255205..43343479hg19UCSC Ensembl
Innerchr19:47947045..48035319hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3888275
hg1988275
hg1888275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065780
Supporting Variants
Samples
Known GenesLOC100289650, PSG10P, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568688
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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