A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569546



Internal ID18867827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42795265..43092807hg38UCSC Ensembl
Innerchr19:43299417..43596959hg19UCSC Ensembl
Innerchr19:47991257..48288799hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38297543
hg19297543
hg18297543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056761
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569546
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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