A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064974



Internal ID19154193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42758818..42857538hg38UCSC Ensembl
Innerchr19:43262970..43361690hg19UCSC Ensembl
Innerchr19:47954810..48053530hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3898721
hg1998721
hg1898721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3555n100
Supporting Variantsnssv3568826, nssv3722865
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)nsv1064974
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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