A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064999



Internal ID19154218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42811447..43307659hg38UCSC Ensembl
Innerchr19:43315599..43811811hg19UCSC Ensembl
Innerchr19:48007439..48503651hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38496213
hg19496213
hg18496213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3566n100
Supporting Variantsnssv3569585
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064999
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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